A novel nonsense mutation in MYO6 is associated with progressive nonsyndromic hearing loss in a Danish DFNA22 family
Research output: Contribution to journal › Journal article › Research › peer-review
Udgivelsesdato: 2008/4/15
Original language | English |
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Journal | American Journal of Medical Genetics. Part A |
Volume | 146A |
Issue number | 8 |
Pages (from-to) | 1017-1025 |
Number of pages | 8 |
ISSN | 1552-4825 |
Publication status | Published - 2008 |
ID: 9566156