Mutations in the human α-tectorin gene cause autosomal dominant non- syndromic hearing impairment

Kristien Verhoeven; Lut Van Laer; Karin Kirschhofer; P. Kevin Legan; David C. Hughes; Isabelle Schatteman; Margriet Verstreken; Peter Van Hauwe; Paul Coucke; Achih Chen; Richard J.H. Smith; Thomas Somers; F. Erwin Offeciers; Paul Van De Heyning; Guy P. Richardson; Franz Wachtler; William J. Kimberling; Patrick J. Willems; Paul J. Govaerts; Guy Van Camp

doi:10.1038/ng0598-60

Mutations in the human α-tectorin gene cause autosomal dominant non- syndromic hearing impairment

Kristien Verhoeven
, Lut Van Laer
, Karin Kirschhofer
, P. Kevin Legan
, David C. Hughes
, Isabelle Schatteman
, Margriet Verstreken
, Peter Van Hauwe
, Paul Coucke
, Achih Chen
, Richard J.H. Smith
, Thomas Somers
, F. Erwin Offeciers
, Paul Van De Heyning
, Guy P. Richardson
, Franz Wachtler
, William J. Kimberling
, Patrick J. Willems
, Paul J. Govaerts
, Guy Van Camp^*

^*Corresponding author for this work

University of Antwerp
Medical University of Vienna
University of Sussex
University of Nottingham
St-Augustinus Hospital
University of Iowa
University of Vienna
Boys Town National Research Hospital

Research output: Contribution to journal › Article › peer-review

321 Citations (SciVal)

Original language	English
Pages (from-to)	60-62
Number of pages	3
Journal	Nature Genetics
Volume	19
Issue number	1
DOIs	https://doi.org/10.1038/ng0598-60
Publication status	Published (VoR) - 1998

Access to Document

10.1038/ng0598-60

Cite this

Verhoeven, K., Van Laer, L., Kirschhofer, K., Legan, P. K., Hughes, D. C., Schatteman, I., Verstreken, M., Van Hauwe, P., Coucke, P., Chen, A., Smith, R. J. H., Somers, T., Offeciers, F. E., Van De Heyning, P., Richardson, G. P., Wachtler, F., Kimberling, W. J., Willems, P. J., Govaerts, P. J., & Van Camp, G. (1998). Mutations in the human α-tectorin gene cause autosomal dominant non- syndromic hearing impairment. Nature Genetics, 19(1), 60-62. https://doi.org/10.1038/ng0598-60

@article{f57e53a70a1f4e16af6b1bb66c217b12,

title = "Mutations in the human α-tectorin gene cause autosomal dominant non- syndromic hearing impairment",

author = "Kristien Verhoeven and \{Van Laer\}, Lut and Karin Kirschhofer and Legan, \{P. Kevin\} and Hughes, \{David C.\} and Isabelle Schatteman and Margriet Verstreken and \{Van Hauwe\}, Peter and Paul Coucke and Achih Chen and Smith, \{Richard J.H.\} and Thomas Somers and Offeciers, \{F. Erwin\} and \{Van De Heyning\}, Paul and Richardson, \{Guy P.\} and Franz Wachtler and Kimberling, \{William J.\} and Willems, \{Patrick J.\} and Govaerts, \{Paul J.\} and \{Van Camp\}, Guy",

year = "1998",

doi = "10.1038/ng0598-60",

language = "English",

volume = "19",

pages = "60--62",

journal = "Nature Genetics",

issn = "1061-4036",

publisher = "Springer Nature",

number = "1",

}

Verhoeven, K, Van Laer, L, Kirschhofer, K, Legan, PK, Hughes, DC, Schatteman, I, Verstreken, M, Van Hauwe, P, Coucke, P, Chen, A, Smith, RJH, Somers, T, Offeciers, FE, Van De Heyning, P, Richardson, GP, Wachtler, F, Kimberling, WJ, Willems, PJ, Govaerts, PJ & Van Camp, G 1998, 'Mutations in the human α-tectorin gene cause autosomal dominant non- syndromic hearing impairment', Nature Genetics, vol. 19, no. 1, pp. 60-62. https://doi.org/10.1038/ng0598-60

TY - JOUR

T1 - Mutations in the human α-tectorin gene cause autosomal dominant non- syndromic hearing impairment

AU - Verhoeven, Kristien

AU - Van Laer, Lut

AU - Kirschhofer, Karin

AU - Legan, P. Kevin

AU - Hughes, David C.

AU - Schatteman, Isabelle

AU - Verstreken, Margriet

AU - Van Hauwe, Peter

AU - Coucke, Paul

AU - Chen, Achih

AU - Smith, Richard J.H.

AU - Somers, Thomas

AU - Offeciers, F. Erwin

AU - Van De Heyning, Paul

AU - Richardson, Guy P.

AU - Wachtler, Franz

AU - Kimberling, William J.

AU - Willems, Patrick J.

AU - Govaerts, Paul J.

AU - Van Camp, Guy

PY - 1998

Y1 - 1998

UR - https://www.scopus.com/pages/publications/17344364928

UR - https://www.scopus.com/pages/publications/17344364928#tab=citedBy

U2 - 10.1038/ng0598-60

DO - 10.1038/ng0598-60

M3 - Article

C2 - 9590290

AN - SCOPUS:17344364928

SN - 1061-4036

VL - 19

SP - 60

EP - 62

JO - Nature Genetics

JF - Nature Genetics

IS - 1

ER -

Mutations in the human α-tectorin gene cause autosomal dominant non- syndromic hearing impairment

Access to Document

Other files and links

Fingerprint

Cite this