Whole-Exome Sequencing to Identify a Novel LMNA Gene Mutation Associated with Inherited Cardiac Conduction Disease

BACKGROUND: Inherited cardiac conduction diseases (CCD) are rare but are caused by mutations in a myriad of genes. Recently, whole-exome sequencing has successfully led to the identification of causal mutations for rare monogenic Mendelian diseases. OBJECTIVE: To investigate the genetic background o...

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Detalhes bibliográficos
Main Authors: Lai, Chun-Chi, Yeh, Yung-Hsin, Hsieh, Wen-Ping, Kuo, Chi-Tai, Wang, Wen-Ching, Chu, Chia-Han, Hung, Chiu-Lien, Cheng, Chia-Yang, Tsai, Hsin-Yi, Lee, Jia-Lin, Tang, Chuan-Yi, Hsu, Lung-An
Formato: Artigo
Idioma:Inglês
Publicado em: Public Library of Science 2013
Assuntos:
Research Article
Acesso em linha:https://ncbi.nlm.nih.gov/pmc/articles/PMC3861486/
https://ncbi.nlm.nih.gov/pubmed/24349489
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1371/journal.pone.0083322
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