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Mutations in connexin31 underlie recessive as well as dominant non-syndromic hearing loss

✍ Scribed by Liu, X.-Z.

Book ID: 124066353
Publisher: Oxford University Press
Year: 2000
Tongue: English
Weight: 231 KB
Volume: 9
Category: Article
ISSN: 0964-6906
DOI: 10.1093/hmg/9.1.63

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