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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Detalles Bibliográficos
Autores principales: 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: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2013
Materias:
Research Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3750053/
https://www.ncbi.nlm.nih.gov/pubmed/23990876
http://dx.doi.org/10.1371/journal.pone.0068692

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3750053/
https://www.ncbi.nlm.nih.gov/pubmed/23990876
http://dx.doi.org/10.1371/journal.pone.0068692

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