Human G6PD variant structural studies: Elucidating the molecular basis of
human G6PD deficiency

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Human G6PD variant structural studies: Elucidating the molecular basis of human G6PD deficiency

Glucose-6-phosphate dehydrogenase deficiency is by far the most prevalent human enzymopathy and is gener�ated by a series of point mutations in the X-linked gene encoding G6PD. The severity of the deficiency relies on the various mutational sites in the gene, affecting the protein structure and fu...

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Bibliographic Details
Main Authors:	Alakbaree, Maysaa, Amran, Sayazwani, Mohd Shamsir, Mohd Shamsir, H. Ahmed, Haron, Hamza, Muaawia, Alonazi, Mona, Warsy, Arjumand, Ab Latif, Nurriza
Format:	Article
Language:	English
Published:	Elsevier 2022
Subjects:	T Technology (General)
Online Access:	http://eprints.uthm.edu.my/7296/ http://eprints.uthm.edu.my/7296/1/J14425_356b302151c30fc112ed7f8ac2a459d3%5B1%5D.pdf

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