Loading...

Genomic structure of the canalicular multispecific organic anion-transporter gene (MRP2/cMOAT) and mutations in the ATP-binding-cassette region in Dubin-Johnson syndrome.

Dubin-Johnson syndrome (DJS) is an autosomal recessive disease characterized by conjugated hyperbilirubinemia. Previous studies of the defects in the human canalicular multispecific organic anion transporter gene (MRP2/cMOAT) in patients with DJS have suggested that the gene defects are responsible...

Fuld beskrivelse

Na minha lista:
Bibliografiske detaljer
Main Authors: Toh, S, Wada, M, Uchiumi, T, Inokuchi, A, Makino, Y, Horie, Y, Adachi, Y, Sakisaka, S, Kuwano, M
Format: Artigo
Sprog:Inglês
Udgivet: 1999
Fag:
Online adgang:https://ncbi.nlm.nih.gov/pmc/articles/PMC1377791/
https://ncbi.nlm.nih.gov/pubmed/10053008
Tags: Tilføj Tag
Ingen Tags, Vær først til at tagge denne postø!