Carrier frequency of the GJB2 mutations that cause hereditary hearing loss in the Japanese population

Hearing impairment is one of the most common sensory disorders that affect ~1 in 1000 children, and half of them are considered to be hereditary. Information about the carrier frequencies of mutations that underlie autosomal recessive disorders is indispensable for accurate genetic counseling to pre...

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Detalhes bibliográficos
Publicado no:J Hum Genet
Main Authors: Taniguchi, Mirei, Matsuo, Hirotaka, Shimizu, Seiko, Nakayama, Akiyoshi, Suzuki, Koji, Hamajima, Nobuyuki, Shinomiya, Nariyoshi, Nishio, Shinya, Kosugi, Shinji, Usami, Shin-ichi, Ito, Juichi, Kitajiri, Shin-ichiro
Formato: Artigo
Idioma:Inglês
Publicado em: Nature Publishing Group 2015
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Original Article
Acesso em linha:https://ncbi.nlm.nih.gov/pmc/articles/PMC4635169/
https://ncbi.nlm.nih.gov/pubmed/26178431
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1038/jhg.2015.82
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