Diagnostic Application of Targeted Resequencing for Familial Nonsyndromic Hearing Loss

Identification of causative genes for hereditary nonsyndromic hearing loss (NSHL) is important to decide treatment modalities and to counsel the patients. Due to the genetic heterogeneity in sensorineural genetic disorders, the high-throughput method can be adapted for the efficient diagnosis. To th...

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Hlavní autoři: Choi, Byung Yoon, Park, Gibeom, Gim, Jungsoo, Kim, Ah Reum, Kim, Bong-Jik, Kim, Hyo-Sang, Park, Joo Hyun, Park, Taesung, Oh, Seung-Ha, Han, Kyu-Hee, Park, Woong-Yang
Médium: Artigo
Jazyk:Inglês
Vydáno: Public Library of Science 2013
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Research Article
On-line přístup:https://ncbi.nlm.nih.gov/pmc/articles/PMC3750053/
https://ncbi.nlm.nih.gov/pubmed/23990876
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1371/journal.pone.0068692
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