A carregar...

Congenital sucrase-isomaltase deficiency. Identification of a glutamine to proline substitution that leads to a transport block of sucrase-isomaltase in a pre-Golgi compartment.

Congenital sucrase-isomaltase deficiency is an example of a disease in which mutant phenotypes generate transport-incompetent molecules. Here, we analyze at the molecular level a phenotype of congenital sucrase-isomaltase deficiency in which sucrase-isomaltase (SI) is not transported to the brush bo...

ver descrição completa

Na minha lista:
Detalhes bibliográficos
Main Authors: Ouwendijk, J, Moolenaar, C E, Peters, W J, Hollenberg, C P, Ginsel, L A, Fransen, J A, Naim, H Y
Formato: Artigo
Idioma:Inglês
Publicado em: 1996
Assuntos:
Acesso em linha:https://ncbi.nlm.nih.gov/pmc/articles/PMC507098/
https://ncbi.nlm.nih.gov/pubmed/8609217
Tags: Adicionar Tag
Sem tags, seja o primeiro a adicionar uma tag!