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CSRP3, p.Arg122*, is responsible for hypertrophic cardiomyopathy in a Chinese family.
J Gene Med. 2022 Jan;24(1):e3390. doi: 10.1002/jgm.3390. Epub 2021 Oct 15.
J Gene Med. 2022.
PMID: 34558151
Familial congenital heart disease caused by a frameshift variant in glyoxylate reductase 1 homolog (GLYR1).
Liang C, Xiang R, Chang SH, Liu MW, Jin JY.
Liang C, et al.
QJM. 2024 Apr 12;117(4):297-299. doi: 10.1093/qjmed/hcad281.
QJM. 2024.
PMID: 38070486
No abstract available.
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