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V677 mutation of methylenetetrahydrofolate reductases and cardiovascular disease in Canadian Inuit

Journal Title: The Lancet (British edition) 1997-04-26, Vol.349 (9060), p.1221-1222
Main Author: Hegele, R A
Other Authors: Tully, C , Young, T K , Connelly, P W
Format: Electronic Article Electronic Article
Language: English
Subjects:
Quelle: Alma/SFX Local Collection
Publisher: England
ID: ISSN: 0140-6736
Link: https://www.ncbi.nlm.nih.gov/pubmed/9130949
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title: V677 mutation of methylenetetrahydrofolate reductases and cardiovascular disease in Canadian Inuit
format: Article
creator:
  • Hegele, R A
  • Tully, C
  • Young, T K
  • Connelly, P W
subjects:
  • Abridged Index Medicus
  • Adult
  • Alleles
  • Canada
  • Cardiovascular Diseases - enzymology
  • Cardiovascular Diseases - genetics
  • Genetic Predisposition to Disease
  • Homocysteine - metabolism
  • Homozygote
  • Humans
  • Inuits - genetics
  • Methylenetetrahydrofolate Reductase (NADPH2)
  • Mutation - genetics
  • Oxidoreductases Acting on CH-NH Group Donors - genetics
  • Prevalence
ispartof: The Lancet (British edition), 1997-04-26, Vol.349 (9060), p.1221-1222
description:
language: eng
source: Alma/SFX Local Collection
identifier: ISSN: 0140-6736
fulltext: fulltext
issn:
  • 0140-6736
  • 1474-547X
url: Link


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subjectAbridged Index Medicus ; Adult ; Alleles ; Canada ; Cardiovascular Diseases - enzymology ; Cardiovascular Diseases - genetics ; Genetic Predisposition to Disease ; Homocysteine - metabolism ; Homozygote ; Humans ; Inuits - genetics ; Methylenetetrahydrofolate Reductase (NADPH2) ; Mutation - genetics ; Oxidoreductases Acting on CH-NH Group Donors - genetics ; Prevalence
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