A novel nonsense mutation in MYO6 is associated with progressive nonsyndromic hearing loss in a Danish DFNA22 family

Research output: Contribution to journalJournal articleResearchpeer-review

Udgivelsesdato: 2008/4/15
Original languageEnglish
JournalAmerican Journal of Medical Genetics. Part A
Volume146A
Issue number8
Pages (from-to)1017-1025
Number of pages8
ISSN1552-4825
Publication statusPublished - 2008

ID: 9566156