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Jalil SF | OMICS International
ISSN: 1747-0862

Journal of Molecular and Genetic Medicine
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Jalil SF


Review Studies of GJB2 Gene in Patients with Hearing Impairment in Pakistan

Deafness is inherited as one of the most frequent type of neurosensory disorder. The specific physiologic mechanisms of the different types of hearing loss are still unknown. Recent studies have listed numerous causative agents for hearing loss. Genetic factors contribute to a greater extent in hearing disability. GJB2 gene is one of the most promi... Read More»

Farooqi N, Khan O, Ellaham S and Jalil SF

Review Article: J Mol Genet Med 2017, 11: 316

DOI: 10.4172/1747-0862.1000316

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