Title : Molecular genetics and control of iron metabolism in hemochromatosis.

Pub. Date : 1998 May

PMID : 9658732






1 Functional Relationships(s)
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1 STATE OF ART AND PERSPECTIVE: HC is now recognized as the genetic disease characterized by the homozygosity for the Cys-->Tyr substitution at position 282 (C282Y) of the HFE protein. Cysteine homeostatic iron regulator Homo sapiens