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A founder TMIE mutation is a frequent cause of hearing loss in southeastern Anatolia.
Sirmaci, A; Oztürkmen-Akay, H; Erbek, S; Incesulu, A; Duman, D; Tasir-Yilmaz, S; Ozdag, H; Tekin, M.
Affiliation
  • Sirmaci A; Division of Clinical Molecular Pathology and Genetics, Department of Pediatrics, Ankara University School of Medicine, Ankara.
Clin Genet ; 75(6): 562-7, 2009 Jun.
Article in En | MEDLINE | ID: mdl-19438934
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Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Point Mutation / Hearing Loss, Sensorineural / Membrane Proteins Type of study: Risk_factors_studies Limits: Humans Country/Region as subject: Asia Language: En Journal: Clin Genet Year: 2009 Document type: Article Country of publication: Dinamarca
Fulltext
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Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Point Mutation / Hearing Loss, Sensorineural / Membrane Proteins Type of study: Risk_factors_studies Limits: Humans Country/Region as subject: Asia Language: En Journal: Clin Genet Year: 2009 Document type: Article Country of publication: Dinamarca