Related Experiment Video
Updated: Sep 25, 2025

03:45
Investigating the Pathogenesis of MYH7 Mutation Gly823Glu in Familial Hypertrophic Cardiomyopathy using a Mouse Model
Published on: August 8, 2022
3.8K
[Clinical and HSD11B2 gene analysis of a patient with apparent mineralocorticoid excess]
1Department of Endocrinology, Genetics and Metabolism, Beijing Children's Hospital, Capital Medical University, National Center for Children's Health, Beijing 100045, China.
Zhonghua Er Ke Za Zhi = Chinese Journal of Pediatrics
|April 30, 2022
Abstract
No abstract available in PubMed .
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