Associated Papers
PHKA1-associated phosphorylase kinase deficiency: a monogenic disorder of exercise intolerance and myalgia.
Koch RL et al.
Npj Genomic Medicine, 2025
Glycogen storage disorder types IX: the mutation spectrum and ethnic distribution.
Geramizadeh B et al.
Orphanet Journal of Rare Diseases, 2024
A rare co-occurrence of phosphorylase kinase deficiency (GSD type IXd) and alpha-glycosidase deficiency (GSD Type II) in a 53-year-old man presenting with an atypical glycogen storage disease phenotype.
Picillo E et al.
Acta Myologica : Myopathies and Cardiomyopathies : Official Journal of the Mediterranean Society of Myology, 2024
Novel PHKA1 mutation in glycogen storage disease type IXD with typical myotonic discharges.
Wang CC et al.
Cns Neuroscience & Therapeutics, 2022
Maximal Multistage Shuttle Run Test-induced Myalgia in a Patient with Muscle Phosphorylase B Kinase Deficiency.
Munekane A et al.
Internal Medicine (tokyo, Japan), 2022
Expanding the clinicopathological-genetic spectrum of glycogen storage disease type IXd by a Chinese neuromuscular center.
Huang K et al.
Frontiers in Neurology, 2022
Myopathy and phosphorylase kinase deficiency caused by a mutation in the PHKA1 gene.
Wuyts W et al.
American Journal of Medical Genetics. Part A, 2005
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