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 |
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Subjects: | QU Biochemistry > Cell biology and genetics WV Otolaryngology |
Divisions: | Reserach Vice-Chancellar Department > Cellular and Molecular Research Center |
Depositing User: | Users 1 not found. |
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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