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Screening for MYO15A gene mutations in autosomal recessive nonsyndromic, GJB2 negative Iranian deaf population

✍ Scribed by Zohreh Fattahi; A. Eliot Shearer; Mojgan Babanejad; Niloofar Bazazzadegan; Seyed Navid Almadani; Nooshin Nikzat; Khadijeh Jalalvand; Sanaz Arzhangi; Fatemehsadat Esteghamat; Rezvan Abtahi; Batool Azadeh; Richard J.H. Smith; Kimia Kahrizi; Hossein Najmabadi

Book ID: 111995067
Publisher: John Wiley and Sons
Year: 2012
Tongue: English
Weight: 1009 KB
Volume: 158A
Category: Article
ISSN: 1552-4825
DOI: 10.1002/ajmg.a.34411

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