没有准备 发表于 2025-3-30 11:07:01
http://reply.papertrans.cn/23/2279/227838/227838_51.png易达到 发表于 2025-3-30 14:44:32
http://reply.papertrans.cn/23/2279/227838/227838_52.pngdagger 发表于 2025-3-30 20:08:07
http://reply.papertrans.cn/23/2279/227838/227838_53.pngSTELL 发表于 2025-3-30 21:31:28
Zusammenfassung und Handlungsempfehlungen,e, hypertension, valvular disease, and congenital heart disease sufficient to explain the observed myocardial abnormality. We describe five main cardiomyopathy subtypes as outlined by the European Society of Cardiology: hypertrophic cardiomyopathy, dilated cardiomyopathy, arrhythmogenic cardiomyopat先兆 发表于 2025-3-31 00:57:35
http://reply.papertrans.cn/23/2279/227838/227838_55.png深陷 发表于 2025-3-31 06:41:27
https://doi.org/10.1007/978-3-658-08575-9as been made in understanding the genetic basis of idiopathic dilated cardiomyopathy (iDCM). Rare variants in >30 genes, some also involved in other cardiomyopathies, muscular dystrophy, or syndromic disease, perturb a diverse set of important myocardial proteins to produce a final DCM phenotype. Re重力 发表于 2025-3-31 09:58:52
http://reply.papertrans.cn/23/2279/227838/227838_57.pngB-cell 发表于 2025-3-31 15:04:49
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