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...

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Autores principales: Toh, S, Wada, M, Uchiumi, T, Inokuchi, A, Makino, Y, Horie, Y, Adachi, Y, Sakisaka, S, Kuwano, M
Formato: Artigo
Lenguaje:Inglês
Publicado: 1999
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Research Article
Acceso en línea:https://ncbi.nlm.nih.gov/pmc/articles/PMC1377791/
https://ncbi.nlm.nih.gov/pubmed/10053008
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