Condition: Congenital atransferrinemia


rs121918681 in INHCAP;TF gene and Congenital atransferrinemia PMID 15466165 2004 Molecular characterization of a third case of human atransferrinemia.

PMID 11110675 2000 Molecular characterization of a case of atransferrinemia.

rs121918679 in TF gene and Congenital atransferrinemia PMID 11110675 2000 Molecular characterization of a case of atransferrinemia.

PMID 15466165 2004 Molecular characterization of a third case of human atransferrinemia.

PMID 11920219 2000 Biochemical and genetic defects underlying human congenital hypotransferrinemia.

PMID 17768112 2007 Effects of plasma transfusion on hepcidin production in human congenital hypotransferrinemia.