Condition: HEMOLYTIC ANEMIA, NONSPHEROCYTIC, DUE TO HEXOKINASE DEFICIENCY
rs137853249
in
HK1
gene and
HEMOLYTIC ANEMIA, NONSPHEROCYTIC, DUE TO HEXOKINASE DEFICIENCY
PMID 12393545
2003 HK Utrecht: missense mutation in the active site of human hexokinase associated with hexokinase deficiency and severe nonspherocytic hemolytic anemia.
PMID 7655856
1995 Hexokinase mutations that produce nonspherocytic hemolytic anemia.