Publication : Diverse point mutations in the human glucose-6-phosphate dehydrogenase gene cause enzyme deficiency and mild or severe hemolytic anemia.

First Author  Vulliamy TJ Year  1988
Journal  Proc Natl Acad Sci U S A Volume  85
Pages  5171-5 PubMed ID  3393536
Issue  14

3 Bio Entities

Id Name Short Name Type
IPR022675 Glucose-6-phosphate dehydrogenase, C-terminal G6P_DH_C Domain
IPR001282 Glucose-6-phosphate dehydrogenase G6P_DH Family
IPR022674 Glucose-6-phosphate dehydrogenase, NAD-binding G6P_DH_NAD-bd Domain

To cite PlanMine, please refer to the following publication:

Rozanski, A., Moon, H., Brandl, H., Martín-Durán, J. M., Grohme, M., Hüttner, K., Bartscherer, K., Henry, I., & Rink, J. C.
PlanMine 3.0—improvements to a mineable resource of flatworm biology and biodiversity
Nucleic Acids Research, gky1070. doi:10.1093/nar/gky1070 (2018)