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- W1997481696 abstract "Anderson-Fabry disease is an X-linked recessive lysosomal storage disease resulting from deficient α-galactosidase A activity. The resulting deposition of glycosphyngolipid can cause abnormalities in a number of organ systems including small fibre neuropathy, disturbances in the conduction system of the heart, and defects in the autonomic nervous control." @default.
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- W1997481696 date "2009-08-01" @default.
- W1997481696 modified "2023-09-27" @default.
- W1997481696 title "P1.10 Autonomic control of heart rate and blood pressure in Anderson–Fabry's disease" @default.
- W1997481696 doi "https://doi.org/10.1016/j.autneu.2009.05.106" @default.
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