A dominant variant in the PDE1C gene is associated with nonsyndromic hearing loss

Identification of genes with variants causing non-syndromic hearing loss (NSHL) is challenging due to genetic heterogeneity. The difficulty is compounded by technical limitations that in the past prevented comprehensive gene identification. Recent advances in technology, using targeted capture and n...

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Опубликовано в: :Hum Genet
Главные авторы: Wang, Li, Feng, Yong, Yan, Denise, Qin, Litao, Grati, M’hamed, Mittal, Rahul, Li, Tao, Sundhari, Abhiraami Kannan, Liu, Yalan, Chapagain, Prem, Blanton, Susan H., Liao, Shixiu, Liu, Xuezhong
Формат: Artigo
Язык:Inglês
Опубликовано: 2018
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Article
Online-ссылка:https://ncbi.nlm.nih.gov/pmc/articles/PMC6560636/
https://ncbi.nlm.nih.gov/pubmed/29860631
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1007/s00439-018-1895-y
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