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Genetic Predisposition to Sporadic Congenital Hearing Loss in a Pediatric Population

Discriminating between inherited and non-inherited sporadic hearing loss is challenging. Here, we attempted to delineate genetic inheritance in simplex cases of severe-to-profound congenital hearing loss in Korean children. Variations in SLC26A4 and GJB2 in 28 children with bilateral severe-to-profo...

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Podrobná bibliografie
Vydáno v:Sci Rep
Hlavní autoři: Jung, Jinsei, Lee, Joon Suk, Cho, Kyeong Jee, Yu, Seyoung, Yoon, Joo-Heon, Yung Gee, Heon, Choi, Jae Young
Médium: Artigo
Jazyk:Inglês
Vydáno: Nature Publishing Group 2017
Témata:
On-line přístup:https://ncbi.nlm.nih.gov/pmc/articles/PMC5382691/
https://ncbi.nlm.nih.gov/pubmed/28383030
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1038/srep45973
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