Genetic Linkage Analysis of 15 DFNB Loci in a Group of Iranian Families with Autosomal Recessive Hearing Loss

BACKGROUND: Hearing loss (HL) is the most frequent sensory birth defect in humans. Autosomal recessive non-syndromic HL (ARNSHL) is the most common type of hereditary HL. It is extremely heterogeneous and over 70 loci (known as DFNB) have been identified. This study was launched to determine the rel...

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Detalles Bibliográficos
Autores principales: Tabatabaiefar, MA, Alasti, F, Zohour, M Montazer, Shariati, L, Farrokhi, E, Farhud, DD, Camp, GV, Noori-Daloii, MR, Chaleshtori, M Hashemzadeh
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Tehran University of Medical Sciences 2011
Materias:
Original Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3481767/
https://www.ncbi.nlm.nih.gov/pubmed/23113071

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