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Volumn 6, Issue 1, 2002, Pages 57-61
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Hyperhomocysteinaemia in a coeliac disease heterozygote for the two common mutations (677C->T and 1298A->C) of the methylenetetrahydrofolate reductase gene. Case report;Hiperhomocysteinemia u chorej na celiakie z polimorficznymi allelami (677C-->T I 1298A-->C) genu reduktazy metylenotetrahydrofolanowej w układzie heterozygotycznym--opis przypadku.
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Author keywords
[No Author keywords available]
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Indexed keywords
ALANINE;
ANTIANEMIC AGENT;
CYSTEINE;
FOLIC ACID;
HOMOCYSTEINE;
IRON;
METHYLENETETRAHYDROFOLATE REDUCTASE (NADPH2);
OXIDOREDUCTASE;
THREONINE;
ADOLESCENT;
ARTICLE;
BLOOD;
CASE REPORT;
CELIAC DISEASE;
DIET THERAPY;
ENZYMOLOGY;
FEMALE;
FOLIC ACID DEFICIENCY;
GENETICS;
HETEROZYGOTE;
HUMAN;
HYPERHOMOCYSTEINEMIA;
MUTATION;
RISK FACTOR;
TIME;
TREATMENT OUTCOME;
ADOLESCENT;
ALANINE;
CELIAC DISEASE;
CYSTEINE;
FEMALE;
FOLIC ACID;
FOLIC ACID DEFICIENCY;
HEMATINICS;
HETEROZYGOTE;
HOMOCYSTEINE;
HUMANS;
HYPERHOMOCYSTEINEMIA;
IRON;
METHYLENETETRAHYDROFOLATE REDUCTASE (NADPH2);
MUTATION;
OXIDOREDUCTASES ACTING ON CH-NH GROUP DONORS;
RISK FACTORS;
THREONINE;
TIME FACTORS;
TREATMENT OUTCOME;
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EID: 0036044889
PISSN: 1428345X
EISSN: None
Source Type: Journal
DOI: None Document Type: Article |
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Times cited : (4)
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References (0)
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