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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...
| Autores principales: | , |
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| Formato: | Online Artículo Texto |
| Lenguaje: | English |
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Springer Netherlands
2010
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| Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3757258/ https://www.ncbi.nlm.nih.gov/pubmed/20628902 http://dx.doi.org/10.1007/s10545-010-9160-0 |