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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Detalles Bibliográficos
Autores principales: Charif, Majida, Boulouiz, Redouane, Bakhechane, Amina, Benrahma, Houda, Nahili, Halima, Eloualid, Abdelmajid, Rouba, Hassan, Kandil, Mostafa, Abidi, Omar, Lenaers, Guy, Barakat, Abdelhamid
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Medknow Publications & Media Pvt Ltd 2013
Materias:
Original Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3841559/
https://www.ncbi.nlm.nih.gov/pubmed/24339547
http://dx.doi.org/10.4103/0971-6866.120828

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3841559/
https://www.ncbi.nlm.nih.gov/pubmed/24339547
http://dx.doi.org/10.4103/0971-6866.120828

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