![PHKA2 novel mutation. (A) The role of glycogen phosphorylase (PYGL) and... | Download Scientific Diagram PHKA2 novel mutation. (A) The role of glycogen phosphorylase (PYGL) and... | Download Scientific Diagram](https://www.researchgate.net/publication/361856096/figure/fig1/AS:1183126416039936@1659090727287/PHKA2-novel-mutation-A-The-role-of-glycogen-phosphorylase-PYGL-and-phosphorylase.png)
PHKA2 novel mutation. (A) The role of glycogen phosphorylase (PYGL) and... | Download Scientific Diagram
![PHKA2 mutation spectrum in Korean patients with glycogen storage disease type IX: prevalence of deletion mutations – topic of research paper in Biological sciences. Download scholarly article PDF and read for free PHKA2 mutation spectrum in Korean patients with glycogen storage disease type IX: prevalence of deletion mutations – topic of research paper in Biological sciences. Download scholarly article PDF and read for free](https://cyberleninka.org/viewer_images/631016/f/1.png)
PHKA2 mutation spectrum in Korean patients with glycogen storage disease type IX: prevalence of deletion mutations – topic of research paper in Biological sciences. Download scholarly article PDF and read for free
![A novel PHKA2 mutation in a Chinese child with glycogen storage disease type IXa: a case report and literature review | BMC Medical Genetics | Full Text A novel PHKA2 mutation in a Chinese child with glycogen storage disease type IXa: a case report and literature review | BMC Medical Genetics | Full Text](https://media.springernature.com/full/springer-static/image/art%3A10.1186%2Fs12881-019-0789-8/MediaObjects/12881_2019_789_Fig1_HTML.png)
A novel PHKA2 mutation in a Chinese child with glycogen storage disease type IXa: a case report and literature review | BMC Medical Genetics | Full Text
![PHKA2 mutation spectrum in Korean patients with glycogen storage disease type IX: prevalence of deletion mutations | BMC Medical Genetics | Full Text PHKA2 mutation spectrum in Korean patients with glycogen storage disease type IX: prevalence of deletion mutations | BMC Medical Genetics | Full Text](https://media.springernature.com/lw685/springer-static/image/art%3A10.1186%2Fs12881-016-0295-1/MediaObjects/12881_2016_295_Fig1_HTML.gif)
PHKA2 mutation spectrum in Korean patients with glycogen storage disease type IX: prevalence of deletion mutations | BMC Medical Genetics | Full Text
![PHKA1/PHKA2 Rabbit anti-Human, Mouse, Rat, Polyclonal, Invitrogen™ 100 μL; Unconjugated Products | Fisher Scientific PHKA1/PHKA2 Rabbit anti-Human, Mouse, Rat, Polyclonal, Invitrogen™ 100 μL; Unconjugated Products | Fisher Scientific](https://assets.fishersci.com/TFS-Assets/LSG/antibodies/PA5-106488-PHKA1-PHKA2-WB-2-20190808102937.jpg-250.jpg)