Novel mutations in the pejvakin gene are associated with autosomal recessive non-syndromic hearing loss in Iranian families

Hashemzadeh Chaleshtori, M. and Simpson, M.A. and Farrokhi, E. and Dolati, M. and Hoghooghi Rad, L. and Amani Geshnigani, S. and Crosby, A.H. (2007) Novel mutations in the pejvakin gene are associated with autosomal recessive non-syndromic hearing loss in Iranian families. CLINICAL GENETICS, 72 (3). pp. 261-263.

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Item Type: Article
Subjects: QU Biochemistry > Cell biology and genetics
WV Otolaryngology
Divisions: Reserach Vice-Chancellar Department > Cellular and Molecular Research Center
Depositing User: zahra bagheri .
Date Deposited: 19 Aug 2017 07:57
Last Modified: 19 Aug 2017 07:57
URI: http://eprints.skums.ac.ir/id/eprint/3160

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