![A novel PHKA1 mutation associating myopathy and cognitive impairment: Expanding the spectrum of phosphorylase kinase b (PhK) deficiency - ScienceDirect A novel PHKA1 mutation associating myopathy and cognitive impairment: Expanding the spectrum of phosphorylase kinase b (PhK) deficiency - ScienceDirect](https://ars.els-cdn.com/content/image/1-s2.0-S0022510X21000848-gr1.jpg)
A novel PHKA1 mutation associating myopathy and cognitive impairment: Expanding the spectrum of phosphorylase kinase b (PhK) deficiency - ScienceDirect
![PHKA1 Rabbit anti-Human, Mouse, Rat, Polyclonal, Proteintech 20 μL; Unconjugated Products | Fisher Scientific PHKA1 Rabbit anti-Human, Mouse, Rat, Polyclonal, Proteintech 20 μL; Unconjugated Products | Fisher Scientific](https://assets.fishersci.com/TFS-Assets/LSG/antibodies/24279-1-AP-PHKA1-WB-b-20190501132214.jpg-650.jpg)
PHKA1 Rabbit anti-Human, Mouse, Rat, Polyclonal, Proteintech 20 μL; Unconjugated Products | Fisher Scientific
![Muscle glycogenosis with low phosphorylase kinase activity: mutations in PHKA1, PHKG1 or six other candidate genes explain only a minority of cases | European Journal of Human Genetics Muscle glycogenosis with low phosphorylase kinase activity: mutations in PHKA1, PHKG1 or six other candidate genes explain only a minority of cases | European Journal of Human Genetics](https://media.springernature.com/lw685/springer-static/image/art%3A10.1038%2Fsj.ejhg.5200996/MediaObjects/41431_2003_Article_BF5200996_Fig3_HTML.gif)