Erratum: A dominant mutation in RPE65 identified by whole-exome sequencing causes retinitis pigmentosa with choroidal involvement (European Journal of Human Genetics (2011) 19 (1074-1081) DOI: 10.1038/ejhg.2011.86)

Sara J. Bowne, Marian M. Humphries, Lori S. Sullivan, Paul F. Kenna, Lawrence C S Tam, Anna S. Kiang, Matthew Campbell, George M. Weinstock, Daniel C. Koboldt, Li Ding, Robert S. Fulton, Erica J. Sodergren, Denis Allman, Sophia Millington-Ward, Arpad Palfi, Alex McKee, Susan H Blanton, Susan Slifer, Ioanna Konidari, G. Jane FarrarStephen P. Daiger, Peter Humphries

Research output: Contribution to journal › Article

Original languageEnglish
JournalEuropean Journal of Human Genetics
Volume19
Issue number10
DOIs
StatePublished - Oct 1 2011
Externally publishedYes

Fingerprint

Exome
Retinitis Pigmentosa
Medical Genetics
Mutation

ASJC Scopus subject areas

  • Genetics(clinical)
  • Genetics

Cite this

Erratum : A dominant mutation in RPE65 identified by whole-exome sequencing causes retinitis pigmentosa with choroidal involvement (European Journal of Human Genetics (2011) 19 (1074-1081) DOI: 10.1038/ejhg.2011.86). / Bowne, Sara J.; Humphries, Marian M.; Sullivan, Lori S.; Kenna, Paul F.; Tam, Lawrence C S; Kiang, Anna S.; Campbell, Matthew; Weinstock, George M.; Koboldt, Daniel C.; Ding, Li; Fulton, Robert S.; Sodergren, Erica J.; Allman, Denis; Millington-Ward, Sophia; Palfi, Arpad; McKee, Alex; Blanton, Susan H; Slifer, Susan; Konidari, Ioanna; Farrar, G. Jane; Daiger, Stephen P.; Humphries, Peter.

In: European Journal of Human Genetics, Vol. 19, No. 10, 01.10.2011.

Research output: Contribution to journal › Article

Bowne, SJ, Humphries, MM, Sullivan, LS, Kenna, PF, Tam, LCS, Kiang, AS, Campbell, M, Weinstock, GM, Koboldt, DC, Ding, L, Fulton, RS, Sodergren, EJ, Allman, D, Millington-Ward, S, Palfi, A, McKee, A, Blanton, SH, Slifer, S, Konidari, I, Farrar, GJ, Daiger, SP & Humphries, P 2011, 'Erratum: A dominant mutation in RPE65 identified by whole-exome sequencing causes retinitis pigmentosa with choroidal involvement (European Journal of Human Genetics (2011) 19 (1074-1081) DOI: 10.1038/ejhg.2011.86)', European Journal of Human Genetics, vol. 19, no. 10. https://doi.org/10.1038/ejhg.2011.132
Bowne SJ, Humphries MM, Sullivan LS, Kenna PF, Tam LCS, Kiang AS et al. Erratum: A dominant mutation in RPE65 identified by whole-exome sequencing causes retinitis pigmentosa with choroidal involvement (European Journal of Human Genetics (2011) 19 (1074-1081) DOI: 10.1038/ejhg.2011.86). European Journal of Human Genetics. 2011 Oct 1;19(10). https://doi.org/10.1038/ejhg.2011.132
Bowne, Sara J. ; Humphries, Marian M. ; Sullivan, Lori S. ; Kenna, Paul F. ; Tam, Lawrence C S ; Kiang, Anna S. ; Campbell, Matthew ; Weinstock, George M. ; Koboldt, Daniel C. ; Ding, Li ; Fulton, Robert S. ; Sodergren, Erica J. ; Allman, Denis ; Millington-Ward, Sophia ; Palfi, Arpad ; McKee, Alex ; Blanton, Susan H ; Slifer, Susan ; Konidari, Ioanna ; Farrar, G. Jane ; Daiger, Stephen P. ; Humphries, Peter. / Erratum : A dominant mutation in RPE65 identified by whole-exome sequencing causes retinitis pigmentosa with choroidal involvement (European Journal of Human Genetics (2011) 19 (1074-1081) DOI: 10.1038/ejhg.2011.86). In: European Journal of Human Genetics. 2011 ; Vol. 19, No. 10.
@article{3cbbefc09d3d42479344b8c2635ad3b1,
title = "Erratum: A dominant mutation in RPE65 identified by whole-exome sequencing causes retinitis pigmentosa with choroidal involvement (European Journal of Human Genetics (2011) 19 (1074-1081) DOI: 10.1038/ejhg.2011.86)",
author = "Bowne, {Sara J.} and Humphries, {Marian M.} and Sullivan, {Lori S.} and Kenna, {Paul F.} and Tam, {Lawrence C S} and Kiang, {Anna S.} and Matthew Campbell and Weinstock, {George M.} and Koboldt, {Daniel C.} and Li Ding and Fulton, {Robert S.} and Sodergren, {Erica J.} and Denis Allman and Sophia Millington-Ward and Arpad Palfi and Alex McKee and Blanton, {Susan H} and Susan Slifer and Ioanna Konidari and Farrar, {G. Jane} and Daiger, {Stephen P.} and Peter Humphries",
year = "2011",
month = "10",
day = "1",
doi = "10.1038/ejhg.2011.132",
language = "English",
volume = "19",
journal = "European Journal of Human Genetics",
issn = "1018-4813",
publisher = "Nature Publishing Group",
number = "10",

}

TY - JOUR

T1 - Erratum

T2 - A dominant mutation in RPE65 identified by whole-exome sequencing causes retinitis pigmentosa with choroidal involvement (European Journal of Human Genetics (2011) 19 (1074-1081) DOI: 10.1038/ejhg.2011.86)

AU - Bowne, Sara J.

AU - Humphries, Marian M.

AU - Sullivan, Lori S.

AU - Kenna, Paul F.

AU - Tam, Lawrence C S

AU - Kiang, Anna S.

AU - Campbell, Matthew

AU - Weinstock, George M.

AU - Koboldt, Daniel C.

AU - Ding, Li

AU - Fulton, Robert S.

AU - Sodergren, Erica J.

AU - Allman, Denis

AU - Millington-Ward, Sophia

AU - Palfi, Arpad

AU - McKee, Alex

AU - Blanton, Susan H

AU - Slifer, Susan

AU - Konidari, Ioanna

AU - Farrar, G. Jane

AU - Daiger, Stephen P.

AU - Humphries, Peter

PY - 2011/10/1

Y1 - 2011/10/1

UR - http://www.scopus.com/inward/record.url?scp=80053072511&partnerID=8YFLogxK

UR - http://www.scopus.com/inward/citedby.url?scp=80053072511&partnerID=8YFLogxK

U2 - 10.1038/ejhg.2011.132

DO - 10.1038/ejhg.2011.132

M3 - Article

AN - SCOPUS:80053072511

VL - 19

JO - European Journal of Human Genetics

JF - European Journal of Human Genetics

SN - 1018-4813

IS - 10

ER -

Access to Document