Erratum: Novel missense mutations of TMPRSS3 in two consanguineous Tunisian families with non-syndromic autosomal recessive deafness (Human Mutation (2201) 18 (101-108))

S. Masmoudi; S. E. Antonarakis; T. Schwede; A. M. Ghorbel; M. Grati; M. P. Pappasavas; M. Drira; A. Elgaied-Boulila; M. Wattenhofer; C. Rossier; H. S. Scott; H. Ayadi; M. Guipponi

doi:10.1002/humu.10048

Erratum: Novel missense mutations of TMPRSS3 in two consanguineous Tunisian families with non-syndromic autosomal recessive deafness (Human Mutation (2201) 18 (101-108))

S. Masmoudi, S. E. Antonarakis, T. Schwede, A. M. Ghorbel, M. Grati, M. P. Pappasavas, M. Drira, A. Elgaied-Boulila, M. Wattenhofer, C. Rossier, H. S. Scott, H. Ayadi, M. Guipponi

Otolaryngology

Research output: Contribution to journal › Comment/debate

Original language	English (US)
Number of pages	1
Journal	Human mutation
Volume	19
Issue number	2
DOIs	https://doi.org/10.1002/humu.10048
State	Published - Feb 13 2002

ASJC Scopus subject areas

Genetics
Genetics(clinical)

Access to Document

10.1002/humu.10048

Cite this

Masmoudi, S., Antonarakis, S. E., Schwede, T., Ghorbel, A. M., Grati, M., Pappasavas, M. P., Drira, M., Elgaied-Boulila, A., Wattenhofer, M., Rossier, C., Scott, H. S., Ayadi, H., & Guipponi, M. (2002). Erratum: Novel missense mutations of TMPRSS3 in two consanguineous Tunisian families with non-syndromic autosomal recessive deafness (Human Mutation (2201) 18 (101-108)). Human mutation, 19(2). https://doi.org/10.1002/humu.10048

Erratum : Novel missense mutations of TMPRSS3 in two consanguineous Tunisian families with non-syndromic autosomal recessive deafness (Human Mutation (2201) 18 (101-108)). / Masmoudi, S.; Antonarakis, S. E.; Schwede, T.; Ghorbel, A. M.; Grati, M.; Pappasavas, M. P.; Drira, M.; Elgaied-Boulila, A.; Wattenhofer, M.; Rossier, C.; Scott, H. S.; Ayadi, H.; Guipponi, M.

In: Human mutation, Vol. 19, No. 2, 13.02.2002.

Research output: Contribution to journal › Comment/debate

Masmoudi, S, Antonarakis, SE, Schwede, T, Ghorbel, AM, Grati, M, Pappasavas, MP, Drira, M, Elgaied-Boulila, A, Wattenhofer, M, Rossier, C, Scott, HS, Ayadi, H & Guipponi, M 2002, 'Erratum: Novel missense mutations of TMPRSS3 in two consanguineous Tunisian families with non-syndromic autosomal recessive deafness (Human Mutation (2201) 18 (101-108))', Human mutation, vol. 19, no. 2. https://doi.org/10.1002/humu.10048

Masmoudi, S. ; Antonarakis, S. E. ; Schwede, T. ; Ghorbel, A. M. ; Grati, M. ; Pappasavas, M. P. ; Drira, M. ; Elgaied-Boulila, A. ; Wattenhofer, M. ; Rossier, C. ; Scott, H. S. ; Ayadi, H. ; Guipponi, M. / Erratum : Novel missense mutations of TMPRSS3 in two consanguineous Tunisian families with non-syndromic autosomal recessive deafness (Human Mutation (2201) 18 (101-108)). In: Human mutation. 2002 ; Vol. 19, No. 2.

@article{c26b924848084f5d9de00f33e17cb023,

title = "Erratum: Novel missense mutations of TMPRSS3 in two consanguineous Tunisian families with non-syndromic autosomal recessive deafness (Human Mutation (2201) 18 (101-108))",

author = "S. Masmoudi and Antonarakis, {S. E.} and T. Schwede and Ghorbel, {A. M.} and M. Grati and Pappasavas, {M. P.} and M. Drira and A. Elgaied-Boulila and M. Wattenhofer and C. Rossier and Scott, {H. S.} and H. Ayadi and M. Guipponi",

year = "2002",

month = feb,

day = "13",

doi = "10.1002/humu.10048",

language = "English (US)",

volume = "19",

journal = "Human Mutation",

issn = "1059-7794",

publisher = "Wiley-Liss Inc.",

number = "2",

}

TY - JOUR

T1 - Erratum

T2 - Novel missense mutations of TMPRSS3 in two consanguineous Tunisian families with non-syndromic autosomal recessive deafness (Human Mutation (2201) 18 (101-108))

AU - Masmoudi, S.

AU - Antonarakis, S. E.

AU - Schwede, T.

AU - Ghorbel, A. M.

AU - Grati, M.

AU - Pappasavas, M. P.

AU - Drira, M.

AU - Elgaied-Boulila, A.

AU - Wattenhofer, M.

AU - Rossier, C.

AU - Scott, H. S.

AU - Ayadi, H.

AU - Guipponi, M.

PY - 2002/2/13

Y1 - 2002/2/13

UR - http://www.scopus.com/inward/record.url?scp=18244404863&partnerID=8YFLogxK

UR - http://www.scopus.com/inward/citedby.url?scp=18244404863&partnerID=8YFLogxK

U2 - 10.1002/humu.10048

DO - 10.1002/humu.10048

M3 - Comment/debate

AN - SCOPUS:18244404863

VL - 19

JO - Human Mutation

JF - Human Mutation

SN - 1059-7794

IS - 2

ER -