Genetic and molecular analysis of the CLDN14 gene in Moroccan family with non-syndromic hearing loss

BACKGROUND: Hearing loss is the most prevalent human genetic sensorineural defect. Mutations in the CLDN14 gene, encoding the tight junction claudin 14 protein expressed in the inner ear, have been shown to cause non-syndromic recessive hearing loss DFNB29. AIM: We describe a Moroccan SF7 family wit...

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Autors principals: Charif, Majida, Boulouiz, Redouane, Bakhechane, Amina, Benrahma, Houda, Nahili, Halima, Eloualid, Abdelmajid, Rouba, Hassan, Kandil, Mostafa, Abidi, Omar, Lenaers, Guy, Barakat, Abdelhamid
Format: Artigo
Idioma:Inglês
Publicat: Medknow Publications & Media Pvt Ltd 2013
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Original Article
Accés en línia:https://ncbi.nlm.nih.gov/pmc/articles/PMC3841559/
https://ncbi.nlm.nih.gov/pubmed/24339547
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.4103/0971-6866.120828
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