Identification of three novel mutations in the PHKA2 gene in Czech patients with X-linked liver glycogenosis
Journal of inherited metabolic disease.
2001 Feb ;
24 (1) :
85-7.
Language English Country United States Media print
Document type Journal Article, Research Support, Non-U.S. Gov't
Persistent link
https://www.medvik.cz/link/pmid11286390
- MeSH
- X Chromosome * MeSH
- Child MeSH
- Adult MeSH
- Phosphorylase Kinase deficiency genetics MeSH
- Genetic Linkage MeSH
- Glycogen Storage Disease genetics MeSH
- Humans MeSH
- Mutation * MeSH
- Check Tag
- Child MeSH
- Adult MeSH
- Humans MeSH
- Male MeSH
- Female MeSH
- Publication type
- Journal Article MeSH
- Research Support, Non-U.S. Gov't MeSH
- Geographicals
- Czech Republic MeSH
- Names of Substances
- Phosphorylase Kinase MeSH
