DFNA8%25252F12 caused by TECTA mutations is the most identif…
DFNA8%25252F12 caused by TECTA mutations is the most identified subtype of nonsyndromic autosomal dominant hearing loss
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Journal:
Human MutationOpens in new Window
Collection:
Wiley Online Library Database Model 2021
Coverage:
- 1996~present
Journal:
Human MutationOpens in new Window
Collection:
Wiley Online Library: Complete Journals
Coverage:
- 1996-01-01~2022-12-01