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Mild hyperhomocysteinemias (>30Umol/l) caused by folate deficiency due to polymorphisms of MTHFR C677T and A1289C in patients from metabolic unit with cardiovascular risk
J. Hyánek, V. Matoška, L. Dubská, B. Míková, H. Pejznochová, J. Dvořáková, L. Táborský, V. Martiniková, J. Privarová
Atherosklerosa ....
2015 ;
() :
18-20.
Language English Country Czech Republic
Persistent link
https://www.medvik.cz/link/bmc16003673
- MeSH
- Adult MeSH
- Homozygote MeSH
- Hyperhomocysteinemia * diagnosis etiology genetics MeSH
- Cardiovascular Diseases prevention & control MeSH
- Folic Acid therapeutic use MeSH
- Middle Aged MeSH
- Humans MeSH
- Methylenetetrahydrofolate Reductase (NADPH2) * genetics deficiency MeSH
- Young Adult MeSH
- Folic Acid Deficiency diagnosis enzymology drug therapy genetics MeSH
- Aged MeSH
- Check Tag
- Adult MeSH
- Middle Aged MeSH
- Humans MeSH
- Young Adult MeSH
- Aged MeSH
Praha, 9.-10. září 2015
Bibliography, etc.Literatura
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