La mutation 35delG du gène de la connexine 26, une cause fréquente des surdités non syndromiques autosomiques récessives au Maroc
Author:
Publisher
Elsevier BV
Subject
Pediatrics, Perinatology and Child Health
Reference14 articles.
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3. Prelingual deafness: high prevalence of a 30delG mutation in the connexion 26 gene;Denoyelle;Hum. Mol. Genet.,1997
4. A non-syndrome form of neurosensory, recessive deafness maps to the pericentromic region of chromosome 13q;Guilford;Nat. Genet.,1994
5. Frequencies of gap- and tight-junction mutations in Turkish families with autosomal-recessive non-syndromic hearing loss;Uyguner;Clin. Genet.,2003
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2. The frequency of the homozygote 35delG mutation in the connexin 26 gene in North African with non-syndromic hearing loss: A meta-analysis study;Meta Gene;2021-06
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4. Enhancing Genetic Medicine: Rapid and Cost-Effective Molecular Diagnosis for a GJB2 Founder Mutation for Hearing Impairment in Ghana;Genes;2020-01-27
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