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Adipocytes participate in storage in α-galactosidase deficiency (Fabry disease)

Ultrastructural and histochemical studies of bioptic and postmortem tissue samples from ten Fabry hemizygotes showed lysosomal storage in adipocytes as a constant feature of the classic phenotype of α-galactosidase (GLA) deficiency. The storage was represented by a crescent-shaped line of storage ly...

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Detalhes bibliográficos
Main Authors: Hůlková, Helena, Elleder, Milan
Formato: Artigo
Idioma:Inglês
Publicado em: Springer Netherlands 2010
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Acesso em linha:https://ncbi.nlm.nih.gov/pmc/articles/PMC3757258/
https://ncbi.nlm.nih.gov/pubmed/20628902
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1007/s10545-010-9160-0
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