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Biochemical and molecular analyses in three patients with 3-hydroxy-3-methylglutaric aciduria
E. Pospíšilová, L. Mrazova, J. Hrda
Language English Country Netherlands
Document type Case Reports
Grant support
NE6003
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
- Hydro-Lyases genetics deficiency MeSH
- Child MeSH
- Research Support as Topic MeSH
- Humans MeSH
- Meglutol urine MeSH
- Check Tag
- Child MeSH
- Humans MeSH
- Publication type
- Case Reports MeSH
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- $a Institute of Inherited Metabolic Diseases, General Faculty Hospital and 1st Faculty of Medicine, Prague, CZ
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- GRA __
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