Prevalence of GJB2 (CX26) gene mutations in south Iranian patients with autosomal recessive nonsyndromic sensorineural hearing loss. [electronic resource]

By: Contributor(s): Producer: 20130409Description: 10481-7 p. digitalISSN:
  • 1573-4978
Subject(s): Online resources: In: Molecular biology reports vol. 39
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Publication Type: Journal Article; Research Support, Non-U.S. Gov't

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