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Updated: Jan 10, 2026

Investigating the Pathogenesis of MYH7 Mutation Gly823Glu in Familial Hypertrophic Cardiomyopathy using a Mouse Model
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Published on: August 8, 2022

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临界儿科心肌病的基因型和表型特征:一项对20名患者的队列研究

Yuanyuan Xu1, Min Li1, Xiaoling Zhao1

  • 1Department of Pediatric Intensive Care Unit, Anhui Provincial Children's Hospital/Children's Medical Center of Anhui Medical University, Hefei 230051, Anhui, China.

Clinica chimica acta; international journal of clinical chemistry
|November 21, 2025
PubMed
概括

儿科心肌病 (PCM) 是儿童心力衰竭的主要原因. 临界病症PCM患者的基因检测显示出高异质性,扩张性心肌病是最常见的亚型.

关键词:
群组研究是一项群组研究.基因检测是一种基因检测.在MYH7中,MYH7是MYH7.儿科心肌病 儿科心肌病在RPL3L中,使用RPL3L.

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