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ENPolyglucosan Body Myopathy 2 (PGBM2)
Alias:
Polyglucosan Body Myopathy Type 2
Pgbm2
Myopathy, Polyglucosan Body, Type 2
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Polyglucosan Body Myopathy 2, also known as polyglucosan body myopathy type 2, is related to glycogen storage disease xv and limb-girdle muscular dystrophy. An important gene associated with Polyglucosan Body Myopathy 2 is GYG1 (Glycogenin 1). Affiliated tissues include skeletal muscle and heart, and related phenotypes are muscle fiber inclusion bodies and muscle fiber polyglucosan inclusion bodies
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MALACARDS
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