Tag : Asian Continental Ancestry Group / genetics

Cardiology

Association of genetic defects in the apelin-AGTRL1 system with myocardial infarction risk in Han Chinese.

Newsemia
Related Articles Association of genetic defects in the apelin-AGTRL1 system with myocardial infarction risk in Han Chinese. Gene. 2021 Jan 15;766:145143 Authors: Li Y, Liu...
Cardiology

A novel TAB2 nonsense mutation (p.S149X) causing autosomal dominant congenital heart defects: a case report of a Chinese family.

Newsemia
Related Articles A novel TAB2 nonsense mutation (p.S149X) causing autosomal dominant congenital heart defects: a case report of a Chinese family. BMC Cardiovasc Disord. 2020...
Cardiology

The association between the D166E polymorphism of the lipoprotein associated phospholipase A2 and risk of myocardial infarction.

Newsemia
Related Articles The association between the D166E polymorphism of the lipoprotein associated phospholipase A2 and risk of myocardial infarction. Eur Rev Med Pharmacol Sci. 2019...
Cardiology

Novel Mutation in MYH6 in 2 Unrelated Chinese Han Families With Familial Atrial Septal Defect.

Newsemia
Related Articles Novel Mutation in MYH6 in 2 Unrelated Chinese Han Families With Familial Atrial Septal Defect. Circ Genom Precis Med. 2019 11;12(11):e002732 Authors: Xia...

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