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
Article, Chapter
Authors:
M.S. Hildebrand
Publication:
Volume:32,
Issue:7,
Page(s):825-834
Published:
2011
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