glycogen storage disease subtype V(English)
- caused by mutation in the gene encoding muscle glycogen phosphorylase, localized to 11q13 by fluorescence in situ hybridization. Also as McArdle disease; myophosphorylase deficiency; muscle glycogen phosphorylase deficiency
- GSD, GSD-I
- Myocyte / muscle, Pathology, Congenital disorders
- https://doi.org…jg.v13.i18.2541
- https://doi.org…83834-6.00097-5