Creation of an iPSC-Based Skeletal Muscle Model of McArdle Disease Harbouring the Mutation c.2392T>C (p.Trp798Arg) in the PYGM Gene.
- Resource Type
- Article
- Source
- Biomedicines; Sep2023, Vol. 11 Issue 9, p2434, 16p
- Subject
SKELETAL muscle GLYCOGEN storage disease type II GLYCOGEN phosphorylase INDUCED pluripotent stem cells - Language
- ISSN
- 22279059