A novel nonsense mutation in TNNT2 in a Chinese pedigree with hypertrophic cardiomyopathy: A case report

RATIONALE: Hypertrophic cardiomyopathy (HCM) is an inherited myocardial disease and a common cause of sudden cardiac death, heart failure, atrial fibrillation and stroke. In families affected by HCM, genotyping is useful for identifying susceptible relatives. In the present study, we investigated th...

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Detaylı Bibliyografya
Yayımlandı:Medicine (Baltimore)
Asıl Yazarlar: Gao, Guangyuan, Liu, Guohui, Chen, Weiwei, Tong, Yaliang, Mao, Cuiying, Liu, Jinsha, Zhang, Xing, He, Max M., Yang, Ping
Materyal Türü: Artigo
Dil:Inglês
Baskı/Yayın Bilgisi: Lippincott Williams & Wilkins 2020
Konular:
3400
Online Erişim:https://ncbi.nlm.nih.gov/pmc/articles/PMC7447477/
https://ncbi.nlm.nih.gov/pubmed/32846832
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1097/MD.0000000000021843
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