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Sequence variants in genes causing nonsyndromic hearing loss in a Pakistani cohort

BACKGROUND: Hearing loss or hearing impairment is a clinically and genetically heterogeneous disorder. More than 117 genes were discovered to date in hereditary, nonsyndromic hearing loss (NSHL). Identifying novel gene variants and their frequency in specific populations is valuable for public healt...

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Podrobná bibliografie
Vydáno v:Mol Genet Genomic Med
Hlavní autoři: Khan, Amjad, Han, Shirui, Wang, Rongrong, Ansar, Muhammad, Ahmad, Wasim, Zhang, Xue
Médium: Artigo
Jazyk:Inglês
Vydáno: John Wiley and Sons Inc. 2019
Témata:
On-line přístup:https://ncbi.nlm.nih.gov/pmc/articles/PMC6732339/
https://ncbi.nlm.nih.gov/pubmed/31389194
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1002/mgg3.917
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