GJB2 (connexin 26) gene mutations in Moroccan patients with autosomal recessive non-syndromic hearing loss and carrier frequency of the common GJB2-35delG mutation.

Abidi, Omar; Boulouiz, Redouane; Nahili, Halima; Ridal, Mohammed; Alami, Mohamed Noureddine; Tlili, Abdelaziz; Rouba, Hassan; Masmoudi, Saber; Chafik, Abdelaziz; Hassar, Mohammed; Barakat, Abdelhamid

Abidi, Omar; Boulouiz, Redouane; Nahili, Halima; Ridal, Mohammed; Alami, Mohamed Noureddine; Tlili, Abdelaziz; Rouba, Hassan; Masmoudi, Saber; Chafik, Abdelaziz; Hassar, Mohammed; Barakat, Abdelhamid.

Affiliation

Abidi O; Laboratoire de Génétique Humaine, Département de Recherche Scientifique, Institut Pasteur, Casablanca, Morocco.

Int J Pediatr Otorhinolaryngol ; 71(8): 1239-45, 2007 Aug.

Article in En | MEDLINE | ID: mdl-17553572

Subject(s)

Connexins/genetics; Genes, Recessive/genetics; Hearing Loss/ethnology; Hearing Loss/genetics; Point Mutation/genetics; Chromosome Mapping; Connexin 26; DNA Mutational Analysis; Gene Deletion; Genetic Carrier Screening/methods; Genotype; Heterozygote; Humans; Morocco; Pedigree; Polymerase Chain Reaction

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Database: MEDLINE Main subject: Point Mutation / Connexins / Genes, Recessive / Hearing Loss Type of study: Risk_factors_studies Limits: Humans Country/Region as subject: Africa Language: En Journal: Int J Pediatr Otorhinolaryngol Year: 2007 Type: Article Affiliation country: Morocco

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