Inhibition of alanine:glyoxylate aminotransferase 1 dimerization is a prerequisite for its peroxisome-to-mitochondrion mistargeting in primary hyperoxaluria type 1

Peroxisome-to-mitochondrion mistargeting of the homodimeric enzyme alanine:glyoxylate aminotransferase 1 (AGT) in the autosomal recessive disease primary hyperoxaluria type 1 (PH1) is associated with the combined presence of a normally occurring Pro(11)Leu polymorphism and a PH1-specific Gly170Arg m...

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Detalles Bibliográficos
Formato: Texto
Lenguaje:English
Publicado: The Rockefeller University Press 1996
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Articles
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2133393/
https://www.ncbi.nlm.nih.gov/pubmed/8922378

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2133393/
https://www.ncbi.nlm.nih.gov/pubmed/8922378

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