A case of human vitamin A deficiency caused by an inherited defect in retinol-binding protein without clinical symptoms except night blindness

scientific article

A case of human vitamin A deficiency caused by an inherited defect in retinol-binding protein without clinical symptoms except night blindness is …
instance of (P31):
scholarly articleQ13442814
review articleQ7318358

External links are
P356DOI10.1111/J.1753-4887.1999.TB06955.X
P698PubMed publication ID10518414

P2093author name stringWolf G
P433issue8
P921main subjectvitamin A deficiencyQ2655893
P304page(s)258-260
P577publication date1999-08-01
P1433published inNutrition ReviewsQ15765213
P1476titleA case of human vitamin A deficiency caused by an inherited defect in retinol-binding protein without clinical symptoms except night blindness
P478volume57

Reverse relations

cites work (P2860)
Q89000215A non-retinoid antagonist of retinol-binding protein 4 rescues phenotype in a model of Stargardt disease without inhibiting the visual cycle
Q92915328Comparative pharmacokinetics and pharmacodynamics of the advanced Retinol-Binding Protein 4 antagonist in dog and cynomolgus monkey
Q91954772Design, Synthesis, and Preclinical Efficacy of Novel Nonretinoid Antagonists of Retinol-Binding Protein 4 in the Mouse Model of Hepatic Steatosis
Q34494040Exome analysis identified a novel mutation in the RBP4 gene in a consanguineous pedigree with retinal dystrophy and developmental abnormalities
Q34074393Pharmacological inhibition of lipofuscin accumulation in the retina as a therapeutic strategy for dry AMD treatment

Search more.