The effects of laforin, malin, Stbd1, and Ptg deficiencies on heart glycogen levels in Pompe disease mouse models

The effects of laforin, malin, Stbd1, and Ptg deficiencies on heart glycogen levels in Pompe disease mouse models

Indiana University-Purdue University Indianapolis (IUPUI) === Pompe disease (PD) is a rare metabolic myopathy characterized by loss of acid alpha-glucosidase (GAA), the enzyme responsible for breaking down glycogen to glucose within the lysosomes. PD cells accumulate massive quantities of glycogen w...

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Bibliographic Details
Main Author: Conway, Betsy Ann
Other Authors: Roach, Peter J.
Language:en
Published: 2016
Subjects:
Pompe disease
STBD1
PTG
EMP2A
EPM2B
Malin
Laforin
Lysosomal glycogen
GAA
Glycogen storage disease type II
Glycogen storage disease type II > Genetic aspects
Glycogen > Metabolism
Lysomal storage disease
Online Access:http://hdl.handle.net/1805/7979

Internet

http://hdl.handle.net/1805/7979

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