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

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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.",

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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

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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

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