Genotype-phenotype correlation for DFNA22: characterization of non-syndromic, autosomal dominant, progressive sensorineural hearing loss due to MYO6 mutations.

V. Topsakal; N. Hilgert; J. van Dinther; L. Tranebjaerg; N.D. Rendtorff; A. Zarowski; E. Offeciers; G. van Camp; P. van de Heyning

doi:10.1159/000255339

Genotype-phenotype correlation for DFNA22: characterization of non-syndromic, autosomal dominant, progressive sensorineural hearing loss due to MYO6 mutations.

Translated title of the contribution: Genotype-phenotype correlation for DFNA22: characterization of non-syndromic, autosomal dominant, progressive sensorineural hearing loss due to MYO6 mutations.

V. Topsakal
, N. Hilgert
, J. van Dinther
, L. Tranebjaerg
, N.D. Rendtorff
, A. Zarowski
, E. Offeciers
, G. van Camp
, P. van de Heyning

Department of Otorhinolaryngology–Head and Neck Surgery

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

Translated title of the contribution	Genotype-phenotype correlation for DFNA22: characterization of non-syndromic, autosomal dominant, progressive sensorineural hearing loss due to MYO6 mutations.
Original language	Undefined/Unknown
Pages (from-to)	211-220
Number of pages	10
Journal	Audiology & Neuro-otology
Volume	15
Issue number	4
DOIs	https://doi.org/10.1159/000255339
Publication status	Published - 2010

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10.1159/000255339

Cite this

Topsakal, V., Hilgert, N., van Dinther, J., Tranebjaerg, L., Rendtorff, N. D., Zarowski, A., Offeciers, E., van Camp, G., & van de Heyning, P. (2010). Genotype-phenotype correlation for DFNA22: characterization of non-syndromic, autosomal dominant, progressive sensorineural hearing loss due to MYO6 mutations. Audiology & Neuro-otology, 15(4), 211-220. https://doi.org/10.1159/000255339

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title = "Genotype-phenotype correlation for DFNA22: characterization of non-syndromic, autosomal dominant, progressive sensorineural hearing loss due to MYO6 mutations.",

author = "V. Topsakal and N. Hilgert and \{van Dinther\}, J. and L. Tranebjaerg and N.D. Rendtorff and A. Zarowski and E. Offeciers and \{van Camp\}, G. and \{van de Heyning\}, P.",

year = "2010",

doi = "10.1159/000255339",

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Topsakal, V, Hilgert, N, van Dinther, J, Tranebjaerg, L, Rendtorff, ND, Zarowski, A, Offeciers, E, van Camp, G & van de Heyning, P 2010, 'Genotype-phenotype correlation for DFNA22: characterization of non-syndromic, autosomal dominant, progressive sensorineural hearing loss due to MYO6 mutations.', Audiology & Neuro-otology, vol. 15, no. 4, pp. 211-220. https://doi.org/10.1159/000255339

TY - JOUR

T1 - Genotype-phenotype correlation for DFNA22: characterization of non-syndromic, autosomal dominant, progressive sensorineural hearing loss due to MYO6 mutations.

AU - Topsakal, V.

AU - Hilgert, N.

AU - van Dinther, J.

AU - Tranebjaerg, L.

AU - Rendtorff, N.D.

AU - Zarowski, A.

AU - Offeciers, E.

AU - van Camp, G.

AU - van de Heyning, P.

PY - 2010

Y1 - 2010

U2 - 10.1159/000255339

DO - 10.1159/000255339

M3 - Article

C2 - 19893302

SN - 1420-3030

VL - 15

SP - 211

EP - 220

JO - Audiology & Neuro-otology

JF - Audiology & Neuro-otology

IS - 4

ER -