A carregar...

Optimization of a Histopathological Biomarker for Sphingomyelin Accumulation in Acid Sphingomyelinase Deficiency

Niemann-Pick disease (types A and B), or acid sphingomyelinase deficiency, is an inherited deficiency of acid sphingomyelinase, resulting in intralysosomal accumulation of sphingomyelin in cells throughout the body, particularly within those of the reticuloendothelial system. These cellular changes...

ver descrição completa

Na minha lista:
Detalhes bibliográficos
Main Authors: Taksir, Tatyana V., Johnson, Jennifer, Maloney, Colleen L., Yandl, Emily, Griffiths, Denise, Thurberg, Beth L., Ryan, Susan
Formato: Artigo
Idioma:Inglês
Publicado em: SAGE Publications 2012
Assuntos:
Acesso em linha:https://ncbi.nlm.nih.gov/pmc/articles/PMC3460358/
https://ncbi.nlm.nih.gov/pubmed/22614361
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1369/0022155412451129
Tags: Adicionar Tag
Sem tags, seja o primeiro a adicionar uma tag!