Title : Comprehensive and differential long-term characterization of the alpha-galactosidase A deficient mouse model of Fabry disease focusing on the sensory system and pain development.

Pub. Date : 2016

PMID : 27145802






1 Functional Relationships(s)
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1 BACKGROUND: Fabry disease is an X-linked lysosomal storage disorder due to impaired activity of alpha-galactosidase A with intracellular accumulation of globotriaosylceramide. globotriaosylceramide galactosidase, alpha Mus musculus