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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Main Authors: 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
Formato: Artigo
Idioma:Inglês
Publicado em: Public Library of Science 2013
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Research Article
Acesso em linha: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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