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Identification of three novel mutations in the PHKA2 gene in Czech patients with X-linked liver glycogenosis
J. Rudolfova, R. Slovackova, M. Trbusek
Journal of inherited metabolic disease.
2001 ;
Roč. 24 (č. 1) :
s. 85-87.
Language English Country Netherlands
Persistent link
https://www.medvik.cz/link/bmc02006896
Grant support
NB5993
MZ0
CEP Register
Digital library NLK
Full text - Část
Source
NLK
ProQuest Central
from 1999-02-01 to 2018-11-30
Health & Medicine (ProQuest)
from 1999-02-01 to 2018-11-30
- MeSH
- X Chromosome MeSH
- Phosphorylase Kinase genetics MeSH
- Glycogen Storage Disease genetics MeSH
- Humans MeSH
- Mutation MeSH
- Check Tag
- Humans MeSH
- Geographicals
- Czech Republic MeSH
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