The frequency of GJB2 mutations and the Delta (GJB6-D13S1830) deletion as a cause of autosomal recessive non-syndromic deafness in the Kurdish population.

Mahdieh, N; Nishimura, C; Ali-Madadi, K; Riazalhosseini, Y; Yazdan, H; Arzhangi, S; Jalalvand, K; Ebrahimi, A; Kazemi, S; Smith, R J H; Najmabadi, H

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The frequency of GJB2 mutations and the Delta (GJB6-D13S1830) deletion as a cause of autosomal recessive non-syndromic deafness in the Kurdish population.

Mahdieh, N; Nishimura, C; Ali-Madadi, K; Riazalhosseini, Y; Yazdan, H; Arzhangi, S; Jalalvand, K; Ebrahimi, A; Kazemi, S; Smith, R J H; Najmabadi, H.

Clin Genet ; 65(6): 506-8, 2004 Jun.

Article in En | MEDLINE | ID: mdl-15151513

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Collection: 01-internacional Database: MEDLINE Main subject: Sequence Deletion / Connexins / Hearing Loss / Mutation Limits: Humans Language: En Journal: Clin Genet Year: 2004 Document type: Article Country of publication:

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Collection: 01-internacional Database: MEDLINE Main subject: Sequence Deletion / Connexins / Hearing Loss / Mutation Limits: Humans Language: En Journal: Clin Genet Year: 2004 Document type: Article Country of publication: