Clinical and laboratory features of patients with myophosphorylase deficiency (McArdle disease). [electronic resource]
Producer: 20111123Description: 1055-8 p. digitalISSN:- 1532-2653
- Adolescent
- Adult
- Amino Acids -- genetics
- Creatine Kinase -- blood
- DNA Mutational Analysis
- Female
- Glycogen Phosphorylase -- genetics
- Glycogen Phosphorylase, Muscle Form -- deficiency
- Glycogen Storage Disease Type V -- diagnosis
- Humans
- Male
- Middle Aged
- Muscle, Skeletal -- pathology
- Mutation -- genetics
- Retrospective Studies
- Young Adult
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Publication Type: Journal Article
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