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

Author:

Hůlková Helena,Elleder Milan

Publisher

Wiley

Subject

Genetics(clinical),Genetics

Reference20 articles.

1. Borisov AB (1982) Changes in lysosomal enzyme activity in the process of L-cell adipocyte differentiation. Tsitologiia 24:1440–1443

2. Desnick RJ, Ioannou YA, Eng CM (2001) Alpha-galactosidase A deficiency: Fabry disease. In: Scriver CR, Beaudet AL, Sly WS, Valle D (eds) The metabolic and molecular bases of inherited disease. McGraw-Hill, New York, pp 3733–3774

3. Du H, Heur M, Duanmu M et al (2001) Lysosomal acid lipase-deficient mice: depletion of white and brown fat, severe hepatosplenomegaly, and shortened life span. J Lipid Res 42:489–500

4. Elleder M (1984) Ito cells in lysosomal storage disorders. An ultrastructural study. Virchows Arch B pathol 46:13–19

5. Elleder M (2010) Subcellular, cellular and organ pathology of Fabry Disease. In: Elstein D, ed. Fabry’s Disease. Springer (in press)

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