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王红艳
Name (Pinyin):wanghongyan
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Academic Achievements
A missense mutation in TCN2 is associated with decreased risk for Congenital Heart Defects and may increase cellular uptake of vitamin B12 via Megalin
Apr 2, 2021
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Journal:
Oncotarget
Document Code:
SY153590
Volume:
8
Issue:
33
Page Number:
55216-55229
Translation or Not:
no
Date of Publication:
Jan 1, 2017
Pre One: Recent Progress in Identifying Genetic and Epigenetic Contributions to Epilepsy
Next One: Association of genetic polymorphisms of de novo nucleotide biosynthesis with increased CHD susceptibility in the northern Chinese population
Apr 2, 2021
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