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...

Descripción completa

Detalles Bibliográficos
Autores principales: 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
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Elsevier 2019
Materias:
Genetics, Genomics and Molecular Biology
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6595892/
https://www.ncbi.nlm.nih.gov/pubmed/31294066
http://dx.doi.org/10.1016/j.dib.2019.104129

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6595892/
https://www.ncbi.nlm.nih.gov/pubmed/31294066
http://dx.doi.org/10.1016/j.dib.2019.104129

Ejemplares similares