Genotype-phenotype correlation for DFNA22: characterization of non-syndromic, autosomal dominant, progressive sensorineural hearing loss due to MYO6 mutations (Q45046976)
Jump to navigation
Jump to search
scientific article published on 5 November 2009
| Language | Label | Description | Also known as |
|---|---|---|---|
| English | Genotype-phenotype correlation for DFNA22: characterization of non-syndromic, autosomal dominant, progressive sensorineural hearing loss due to MYO6 mutations |
scientific article published on 5 November 2009 |
Statements
1 reference
Genotype-phenotype correlation for DFNA22: characterization of non-syndromic, autosomal dominant, progressive sensorineural hearing loss due to MYO6 mutations (English)
1 reference
1 reference
1 reference
Vedat Topsakal
1 reference
Nele Hilgert
1 reference
Joost van Dinther
1 reference
Lisbeth Tranebjaerg
1 reference
Nanna D Rendtorff
1 reference
Andrzej Zarowski
1 reference
Erwin Offeciers
1 reference
5 November 2009
1 reference
1 reference
15
1 reference
4
1 reference
211-220
1 reference
Identifiers
1 reference
1 reference