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A rare novel mutation inTECTAcauses autosomal dominant nonsyndromic hearing loss in a Mongolian family

✍ Scribed by Bai, Haihua; Yang, Xukui; Temuribagen, ; Guilan, ; Suyalatu, ; Narisu, Narisu; Wu, Huiguang; Chen, Yujie; Liu, Yangjian; Wu, Qizhu

Book ID: 125398564
Publisher: BioMed Central
Year: 2014
Tongue: English
Weight: 802 KB
Volume: 15
Category: Article
ISSN: 1471-2350
DOI: 10.1186/1471-2350-15-34

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