DFNA8%252F12 caused by TECTA mutations is the most identifie…
DFNA8%252F12 caused by TECTA mutations is the most identified subtype of nonsyndromic autosomal dominant hearing loss
Article, Chapter
Full text availability for this item
Journal:
Human MutationOpens in new Window
Coverage:
- 1996~present; volume:7~present;issue:1~present
Journal:
Human MutationOpens in new Window
Coverage:
- 1996-01-01~present; volume:7~present;issue:1~present