Sign in
  Edit search
DFNA8%2F12 caused by TECTA mutations is the most identified …
DFNA8%2F12 caused by TECTA mutations is the most identified subtype of nonsyndromic autosomal dominant hearing loss
DFNA8%2F12 caused by TECTA mutations is the most identified subtype of nonsyndromic autosomal dominant hearing loss
Article, Chapter
Authors: M.S. Hildebrand
Publication: Human Mutation, Volume:32, Issue:7, Page(s):-834
Published: Wiley, 2011
ISSN: 1059-7794
  Full text availability for this item
View Full Text Source:Human Mutation,Human Mutation,Wiley Online Library Database Model 2021 Opens in new Window
Journal:  Human Mutation Source:Wiley Online Library Database Model 2021 Opens in new Window
Collection:  Wiley Online Library Database Model 2021 Opens in new Window
Coverage:
  • 1996~present; volume:7~present;issue:1~present
View Full Text Source:Human Mutation,Human Mutation,Wiley Online Library: Complete Journals Opens in new Window
Journal:  Human Mutation Source:Wiley Online Library: Complete Journals Opens in new Window
Collection:  Wiley Online Library: Complete Journals Opens in new Window
Coverage:
  • 1996-01-01~present; volume:7~present;issue:1~present
Browse related articles
  Print copies at your library
Check availability in RUQuest
  Request a copy of this item
Cite this item