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Whole-exome sequencing to identify a novel LMNA gene mutation associated with inherited cardiac conduction disease.
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.
Afiliação
  • Lai CC; Department of Computer Science, National Tsing Hua University, Hsinchu, Taiwan.
  • Yeh YH; First Cardiovascular Division, Chang Gung Memorial Hospital, Chang Gung University College of Medicine, Tao-Yuan, Taiwan.
  • Hsieh WP; Institute of Statistics, National Tsing Hua University, Hsinchu, Taiwan.
  • Kuo CT; First Cardiovascular Division, Chang Gung Memorial Hospital, Chang Gung University College of Medicine, Tao-Yuan, Taiwan.
  • Wang WC; Institute of Molecular and Cellular Biology and Department of Life Sciences, National Tsing-Hua University, Hsinchu, Taiwan ; Biomedical Science and Engineering Center, National Tsing Hua University, Hsinchu, Taiwan.
  • Chu CH; Biomedical Science and Engineering Center, National Tsing Hua University, Hsinchu, Taiwan.
  • Hung CL; Institute of Molecular and Cellular Biology and Department of Life Sciences, National Tsing-Hua University, Hsinchu, Taiwan ; Biomedical Science and Engineering Center, National Tsing Hua University, Hsinchu, Taiwan.
  • Cheng CY; Department of Computer Science, National Tsing Hua University, Hsinchu, Taiwan ; Biomedical Science and Engineering Center, National Tsing Hua University, Hsinchu, Taiwan.
  • Tsai HY; First Cardiovascular Division, Chang Gung Memorial Hospital, Chang Gung University College of Medicine, Tao-Yuan, Taiwan.
  • Lee JL; Institute of Molecular and Cellular Biology and Department of Life Sciences, National Tsing-Hua University, Hsinchu, Taiwan.
  • Tang CY; Department of Computer Science, National Tsing Hua University, Hsinchu, Taiwan.
  • Hsu LA; First Cardiovascular Division, Chang Gung Memorial Hospital, Chang Gung University College of Medicine, Tao-Yuan, Taiwan.
PLoS One ; 8(12): e83322, 2013.
Article em En | MEDLINE | ID: mdl-24349489
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Linhagem / Arritmias Cardíacas / Mutação de Sentido Incorreto / Lamina Tipo A / Exoma / Sistema de Condução Cardíaco / Doenças Genéticas Inatas Tipo de estudo: Prognostic_studies / Risk_factors_studies Limite: Adult / Aged / Aged80 / Female / Humans / Male / Middle aged Idioma: En Revista: PLoS One Assunto da revista: CIENCIA / MEDICINA Ano de publicação: 2013 Tipo de documento: Article País de afiliação: Taiwan
Texto completo
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XML
PubMed Links
Buscar no Google

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Linhagem / Arritmias Cardíacas / Mutação de Sentido Incorreto / Lamina Tipo A / Exoma / Sistema de Condução Cardíaco / Doenças Genéticas Inatas Tipo de estudo: Prognostic_studies / Risk_factors_studies Limite: Adult / Aged / Aged80 / Female / Humans / Male / Middle aged Idioma: En Revista: PLoS One Assunto da revista: CIENCIA / MEDICINA Ano de publicação: 2013 Tipo de documento: Article País de afiliação: Taiwan