Source: CTD_human

Gene Disease Score gda Association Type Original DB Sentence supporting the association PMID PMID Year
Entrez Id: 5950
Gene Symbol: RBP4
RBP4
CUI: C0042842
Disease: Vitamin A Deficiency
Vitamin A Deficiency 		0.320 Biomarker CTD_human Biochemical basis for retinol deficiency induced by the I41N and G75D mutations in human plasma retinol-binding protein. 16157297

2005