Erratum

Truncating Mutations in UBAP1 Cause Hereditary Spastic Paraplegia (The American Journal of Human Genetics (2019)104(4)(767–773), (S0002929719300977), (10.1016/j.ajhg.2019.03.001))

Mohammad Ali Farazi Fard, Adriana P. Rebelo, Elena Buglo, Hamid Nemati, Hassan Dastsooz, Ina Gehweiler, Selina Reich, Jennifer Reichbauer, Beatriz Quintáns, Andrés Ordóñez-Ugalde, Andrea Cortese, Steve Courel, Lisa Abreu, Eric Powell, Matt C. Danzi, Nicole B. Martuscelli, Dana M. Bis-Brewer, Feifei Tao, Fariba Zarei, Parham Habibzadeh & 22 others Majid Yavarian, Farzaneh Modarresi, Mohammad Silawi, Zahra Tabatabaei, Masoume Yousefi, Hamid Reza Farpour, Christoph Kessler, Elisabeth Mangold, Xenia Kobeleva, Ivailo Tournev, Teodora Chamova, Amelie J. Mueller, Tobias B. Haack, Mark Tarnopolsky, Ziv Gan-Or, Guy A. Rouleau, Matthis Synofzik, María Jesús Sobrido, Albena Jordanova, Rebecca Schüle, Stephan L Zuchner, Mohammad A Faghihi

Research output: Contribution to journalComment/debate

Abstract

(The American Journal of Human Genetics 104, 767–773; April 4, 2019)In the originally published version of this article, authors Ivailo Tournev and Teodora Chamova were mistakenly omitted from the author list. Their names have been added here. The online version of the full article now appears correctly and includes affiliations for the added authors as well as corrections to some of the other affiliations. The authors regret these omissions.

Original languageEnglish (US)
JournalAmerican journal of human genetics
DOIs
StatePublished - Jan 1 2019

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Hereditary Spastic Paraplegia
Medical Genetics
Names
Emotions
Mutation

ASJC Scopus subject areas

  • Genetics
  • Genetics(clinical)

Cite this

Erratum : Truncating Mutations in UBAP1 Cause Hereditary Spastic Paraplegia (The American Journal of Human Genetics (2019)104(4)(767–773), (S0002929719300977), (10.1016/j.ajhg.2019.03.001)). / Farazi Fard, Mohammad Ali; Rebelo, Adriana P.; Buglo, Elena; Nemati, Hamid; Dastsooz, Hassan; Gehweiler, Ina; Reich, Selina; Reichbauer, Jennifer; Quintáns, Beatriz; Ordóñez-Ugalde, Andrés; Cortese, Andrea; Courel, Steve; Abreu, Lisa; Powell, Eric; Danzi, Matt C.; Martuscelli, Nicole B.; Bis-Brewer, Dana M.; Tao, Feifei; Zarei, Fariba; Habibzadeh, Parham; Yavarian, Majid; Modarresi, Farzaneh; Silawi, Mohammad; Tabatabaei, Zahra; Yousefi, Masoume; Farpour, Hamid Reza; Kessler, Christoph; Mangold, Elisabeth; Kobeleva, Xenia; Tournev, Ivailo; Chamova, Teodora; Mueller, Amelie J.; Haack, Tobias B.; Tarnopolsky, Mark; Gan-Or, Ziv; Rouleau, Guy A.; Synofzik, Matthis; Sobrido, María Jesús; Jordanova, Albena; Schüle, Rebecca; Zuchner, Stephan L; Faghihi, Mohammad A.

In: American journal of human genetics, 01.01.2019.

Research output: Contribution to journalComment/debate

Farazi Fard, MA, Rebelo, AP, Buglo, E, Nemati, H, Dastsooz, H, Gehweiler, I, Reich, S, Reichbauer, J, Quintáns, B, Ordóñez-Ugalde, A, Cortese, A, Courel, S, Abreu, L, Powell, E, Danzi, MC, Martuscelli, NB, Bis-Brewer, DM, Tao, F, Zarei, F, Habibzadeh, P, Yavarian, M, Modarresi, F, Silawi, M, Tabatabaei, Z, Yousefi, M, Farpour, HR, Kessler, C, Mangold, E, Kobeleva, X, Tournev, I, Chamova, T, Mueller, AJ, Haack, TB, Tarnopolsky, M, Gan-Or, Z, Rouleau, GA, Synofzik, M, Sobrido, MJ, Jordanova, A, Schüle, R, Zuchner, SL & Faghihi, MA 2019, 'Erratum: Truncating Mutations in UBAP1 Cause Hereditary Spastic Paraplegia (The American Journal of Human Genetics (2019)104(4)(767–773), (S0002929719300977), (10.1016/j.ajhg.2019.03.001))', American journal of human genetics. https://doi.org/10.1016/j.ajhg.2019.05.009
Farazi Fard, Mohammad Ali ; Rebelo, Adriana P. ; Buglo, Elena ; Nemati, Hamid ; Dastsooz, Hassan ; Gehweiler, Ina ; Reich, Selina ; Reichbauer, Jennifer ; Quintáns, Beatriz ; Ordóñez-Ugalde, Andrés ; Cortese, Andrea ; Courel, Steve ; Abreu, Lisa ; Powell, Eric ; Danzi, Matt C. ; Martuscelli, Nicole B. ; Bis-Brewer, Dana M. ; Tao, Feifei ; Zarei, Fariba ; Habibzadeh, Parham ; Yavarian, Majid ; Modarresi, Farzaneh ; Silawi, Mohammad ; Tabatabaei, Zahra ; Yousefi, Masoume ; Farpour, Hamid Reza ; Kessler, Christoph ; Mangold, Elisabeth ; Kobeleva, Xenia ; Tournev, Ivailo ; Chamova, Teodora ; Mueller, Amelie J. ; Haack, Tobias B. ; Tarnopolsky, Mark ; Gan-Or, Ziv ; Rouleau, Guy A. ; Synofzik, Matthis ; Sobrido, María Jesús ; Jordanova, Albena ; Schüle, Rebecca ; Zuchner, Stephan L ; Faghihi, Mohammad A. / Erratum : Truncating Mutations in UBAP1 Cause Hereditary Spastic Paraplegia (The American Journal of Human Genetics (2019)104(4)(767–773), (S0002929719300977), (10.1016/j.ajhg.2019.03.001)). In: American journal of human genetics. 2019.
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title = "Erratum: Truncating Mutations in UBAP1 Cause Hereditary Spastic Paraplegia (The American Journal of Human Genetics (2019)104(4)(767–773), (S0002929719300977), (10.1016/j.ajhg.2019.03.001))",
abstract = "(The American Journal of Human Genetics 104, 767–773; April 4, 2019)In the originally published version of this article, authors Ivailo Tournev and Teodora Chamova were mistakenly omitted from the author list. Their names have been added here. The online version of the full article now appears correctly and includes affiliations for the added authors as well as corrections to some of the other affiliations. The authors regret these omissions.",
author = "{Farazi Fard}, {Mohammad Ali} and Rebelo, {Adriana P.} and Elena Buglo and Hamid Nemati and Hassan Dastsooz and Ina Gehweiler and Selina Reich and Jennifer Reichbauer and Beatriz Quint{\'a}ns and Andr{\'e}s Ord{\'o}{\~n}ez-Ugalde and Andrea Cortese and Steve Courel and Lisa Abreu and Eric Powell and Danzi, {Matt C.} and Martuscelli, {Nicole B.} and Bis-Brewer, {Dana M.} and Feifei Tao and Fariba Zarei and Parham Habibzadeh and Majid Yavarian and Farzaneh Modarresi and Mohammad Silawi and Zahra Tabatabaei and Masoume Yousefi and Farpour, {Hamid Reza} and Christoph Kessler and Elisabeth Mangold and Xenia Kobeleva and Ivailo Tournev and Teodora Chamova and Mueller, {Amelie J.} and Haack, {Tobias B.} and Mark Tarnopolsky and Ziv Gan-Or and Rouleau, {Guy A.} and Matthis Synofzik and Sobrido, {Mar{\'i}a Jes{\'u}s} and Albena Jordanova and Rebecca Sch{\"u}le and Zuchner, {Stephan L} and Faghihi, {Mohammad A}",
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T2 - Truncating Mutations in UBAP1 Cause Hereditary Spastic Paraplegia (The American Journal of Human Genetics (2019)104(4)(767–773), (S0002929719300977), (10.1016/j.ajhg.2019.03.001))

AU - Farazi Fard, Mohammad Ali

AU - Rebelo, Adriana P.

AU - Buglo, Elena

AU - Nemati, Hamid

AU - Dastsooz, Hassan

AU - Gehweiler, Ina

AU - Reich, Selina

AU - Reichbauer, Jennifer

AU - Quintáns, Beatriz

AU - Ordóñez-Ugalde, Andrés

AU - Cortese, Andrea

AU - Courel, Steve

AU - Abreu, Lisa

AU - Powell, Eric

AU - Danzi, Matt C.

AU - Martuscelli, Nicole B.

AU - Bis-Brewer, Dana M.

AU - Tao, Feifei

AU - Zarei, Fariba

AU - Habibzadeh, Parham

AU - Yavarian, Majid

AU - Modarresi, Farzaneh

AU - Silawi, Mohammad

AU - Tabatabaei, Zahra

AU - Yousefi, Masoume

AU - Farpour, Hamid Reza

AU - Kessler, Christoph

AU - Mangold, Elisabeth

AU - Kobeleva, Xenia

AU - Tournev, Ivailo

AU - Chamova, Teodora

AU - Mueller, Amelie J.

AU - Haack, Tobias B.

AU - Tarnopolsky, Mark

AU - Gan-Or, Ziv

AU - Rouleau, Guy A.

AU - Synofzik, Matthis

AU - Sobrido, María Jesús

AU - Jordanova, Albena

AU - Schüle, Rebecca

AU - Zuchner, Stephan L

AU - Faghihi, Mohammad A

PY - 2019/1/1

Y1 - 2019/1/1

N2 - (The American Journal of Human Genetics 104, 767–773; April 4, 2019)In the originally published version of this article, authors Ivailo Tournev and Teodora Chamova were mistakenly omitted from the author list. Their names have been added here. The online version of the full article now appears correctly and includes affiliations for the added authors as well as corrections to some of the other affiliations. The authors regret these omissions.

AB - (The American Journal of Human Genetics 104, 767–773; April 4, 2019)In the originally published version of this article, authors Ivailo Tournev and Teodora Chamova were mistakenly omitted from the author list. Their names have been added here. The online version of the full article now appears correctly and includes affiliations for the added authors as well as corrections to some of the other affiliations. The authors regret these omissions.

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JF - American Journal of Human Genetics

SN - 0002-9297

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