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...
| Main Authors: | , , , , , , , |
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| Format: | Article |
| Language: | English |
| Published: |
Elsevier
2022
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| Subjects: | |
| Online Access: | http://eprints.uthm.edu.my/7296/1/J14425_356b302151c30fc112ed7f8ac2a459d3%5B1%5D.pdf |