Search Results - Seyed Navid Almadani
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Screening for <i>MYO15A</i> gene mutations in autosomal recessive nonsyndromic, <i>GJB2</i> negative Iranian deaf population 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. Smith, Kimia Kahrizi, Hossein Najmabadi
Published 2012Artigo