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Genetic basis of cardiomyopathy and the genotypes involved in prognosis and left ventricular reverse remodeling

Dilated cardiomyopathy (DCM) and hypertrophic cardiomyopathy (HCM) are genetically and phenotypically heterogeneous. Cardiac function is improved after treatment in some cardiomyopathy patients, but little is known about genetic predictors of long-term outcomes and myocardial recovery following medi...

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Detalles Bibliográficos
Autores principales: Tobita, Takashige, Nomura, Seitaro, Fujita, Takanori, Morita, Hiroyuki, Asano, Yoshihiro, Onoue, Kenji, Ito, Masamichi, Imai, Yasushi, Suzuki, Atsushi, Ko, Toshiyuki, Satoh, Masahiro, Fujita, Kanna, Naito, Atsuhiko T, Furutani, Yoshiyuki, Toko, Haruhiro, Harada, Mutsuo, Amiya, Eisuke, Hatano, Masaru, Takimoto, Eiki, Shiga, Tsuyoshi, Nakanishi, Toshio, Sakata, Yasushi, Ono, Minoru, Saito, Yoshihiko, Takashima, Seiji, Hagiwara, Nobuhisa, Aburatani, Hiroyuki, Komuro, Issei
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5792481/
https://www.ncbi.nlm.nih.gov/pubmed/29386531
http://dx.doi.org/10.1038/s41598-018-20114-9

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