Prediction of functional consequences of the five newly discovered G6PD variations in Taiwan

Glucose-6-phosphate dehydrogenase deficiency (G6PD deficiency; OMIM #300908) is the most common inborn error disorders worldwide. While the G6PD is the key enzyme of removing oxidative stress in erythrocytes, the early diagnosis is utmost vital to prevent chronic and drug-, food- or infection-induce...

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Bibliografiske detaljer
Udgivet i:Data Brief
Main Authors: Chiu, Yen-Hui, Liu, Yu-Ning, Chen, Hsiao-Jan, Chang, Ying-Chen, Kao, Shu-Min, Liu, Mei-Ying, Weng, Ying-Yen, Hsiao, Kwang-Jen, Liu, Tze-Tze
Format: Artigo
Sprog:Inglês
Udgivet: Elsevier 2019
Fag:
Genetics, Genomics and Molecular Biology
Online adgang:https://ncbi.nlm.nih.gov/pmc/articles/PMC6595892/
https://ncbi.nlm.nih.gov/pubmed/31294066
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1016/j.dib.2019.104129
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