Congenital Hemolytic Anemia Due to Hexokinase Deficiency
Overview
Overview
Journal
Am J Dis Child
Publisher
American Medical Association
Specialty
Pediatrics
Date
1978 Jun 1
PMID
655151
Citations
1
Authors
Authors
Affiliations
Affiliations
Soon will be listed here.
Citing Articles
Bartnik M, Pawlik W, Burzynska B, Wasilewski K, Kamienska E, Urasinski T Genes (Basel). 2025; 15(12.
PMID: 39766843 PMC: 11675319. DOI: 10.3390/genes15121576.
De novo variants in HK1 associated with neurodevelopmental abnormalities and visual impairment.
Okur V, Cho M, van Wijk R, van Oirschot B, Picker J, Coury S Eur J Hum Genet. 2019; 27(7):1081-1089.
PMID: 30778173 PMC: 6777464. DOI: 10.1038/s41431-019-0366-9.