RAF1 mutations in childhood-onset dilated cardiomyopathy

Dilated cardiomyopathy (DCM) is a highly heterogeneous trait with sarcomeric gene mutations predominating. The cause of a significant percentage of DCM remains unknown and no gene-specific therapy is available. Based on resequencing with 513 DCM cases and 1,150 matched controls from various ethnical...

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Detalhes bibliográficos
Main Authors: Dhandapany, Perundurai S., Razzaque, Md. Abdur, Muthusami, Uthiralingam, Kunnoth, Sreejith, Edwards, Jonathan J., Mulero-Navarro, Sonia, Riess, Ilan, Pardo, Sherly, Sheng, Jipo, Rani, Deepa Selvi, Rani, Bindhu, Govindaraj, Periyasamy, Flex, Elisabetta, Yokota, Tomohiro, Furutani, Michiko, Nishizawa, Tsutomu, Nakanishi, Toshio, Robbins, Jeffrey, Limongelli, Giuseppe, Hajjar, Roger J., Lebeche, Djamel, Bahl, Ajay, Khullar, Madhu, Rathinavel, Andiappan, Sadler, Kirsten C., Tartaglia, Marco, Matsuoka, Rumiko, Thangaraj, Kumarasamy, Gelb, Bruce D.
Formato: Artigo
Idioma:Inglês
Publicado em: 2014
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Article
Acesso em linha:https://ncbi.nlm.nih.gov/pmc/articles/PMC4049514/
https://ncbi.nlm.nih.gov/pubmed/24777450
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1038/ng.2963
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