Mutations of human TMHS cause recessively inherited non‐syndromic hearing loss

BACKGROUND: Approximately half the cases of prelingual hearing loss are caused by genetic factors. Identification of genes causing deafness is a crucial first step in understanding the normal function of these genes in the auditory system. Recently, a mutant allele of Tmhs was reported to be associa...

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Autors principals: Shabbir, M I, Ahmed, Z M, Khan, S Y, Riazuddin, Saima, Waryah, A M, Khan, S N, Camps, R D, Ghosh, M, Kabra, M, Belyantseva, I A, Friedman, T B, Riazuddin, Sheikh
Format: Artigo
Idioma:Inglês
Publicat: BMJ Group 2006
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Original Article
Accés en línia:https://ncbi.nlm.nih.gov/pmc/articles/PMC2564584/
https://ncbi.nlm.nih.gov/pubmed/16459341
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1136/jmg.2005.039834
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