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A novel DFNA5 mutation, IVS8+4 A>G, in the splice donor site of intron 8 causes late-onset non-syndromic hearing loss in a Chinese family

✍ Scribed by J Cheng; DY Han; P Dai; HJ Sun; R Tao; Q Sun; D Yan; W Qin; HY Wang; XM Ouyang; SZ Yang; JY Cao; GY Feng; LL Du; YZ Zhang; SQ Zhai; WY Yang; XZ Liu; L He; HJ Yuan

Book ID: 110888483
Publisher: John Wiley and Sons
Year: 2007
Tongue: English
Weight: 496 KB
Volume: 72
Category: Article
ISSN: 0009-9163
DOI: 10.1111/j.1399-0004.2007.00889.x

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