A carregar...

Localization of the Wilson’s disease protein product to mitochondria

Wilson’s disease (WND) is an inherited disorder of copper homeostasis characterized by abnormal accumulation of copper in several tissues, particularly in the liver, brain, and kidney. The disease-associated gene encodes a copper-transporting P-type ATPase, the WND protein, the subcellular location...

ver descrição completa

Na minha lista:
Detalhes bibliográficos
Main Authors: Lutsenko, Svetlana, Cooper, Matthew J.
Formato: Artigo
Idioma:Inglês
Publicado em: The National Academy of Sciences 1998
Assuntos:
Acesso em linha:https://ncbi.nlm.nih.gov/pmc/articles/PMC27575/
https://ncbi.nlm.nih.gov/pubmed/9600907
Tags: Adicionar Tag
Sem tags, seja o primeiro a adicionar uma tag!