Source:http://linkedlifedata.com/resource/pubmed/id/12689549
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Predicate | Object |
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rdf:type | |
lifeskim:mentions | |
pubmed:issue |
12
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pubmed:dateCreated |
2003-4-11
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pubmed:abstractText |
The etiology of neural tube defects (NTDs) is multifactorial. The presence of mutated genotypes of C677T and A1298C polymorphisms, and their combined heterozygosity, have been considered risk factors for the occurrence and recurrence of NTDs in some populations. Subjects and method: This case-control study included 159 healthy controls, 27 NTDs patients, 28 patients' mothers and 23 siblings. The polymorphism study was performed by PCR. For fragment digestion, we used the restriction enzymes Hinf I (C677T) and Mbo II (A1298C).
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pubmed:language |
spa
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pubmed:journal | |
pubmed:citationSubset |
IM
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pubmed:chemical | |
pubmed:status |
MEDLINE
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pubmed:month |
Apr
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pubmed:issn |
0025-7753
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pubmed:author | |
pubmed:issnType |
Print
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pubmed:day |
5
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pubmed:volume |
120
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pubmed:owner |
NLM
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pubmed:authorsComplete |
Y
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pubmed:pagination |
441-5
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pubmed:dateRevised |
2009-11-3
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pubmed:meshHeading |
pubmed-meshheading:12689549-Case-Control Studies,
pubmed-meshheading:12689549-Genotype,
pubmed-meshheading:12689549-Humans,
pubmed-meshheading:12689549-Methylenetetrahydrofolate Reductase (NADPH2),
pubmed-meshheading:12689549-Neural Tube Defects,
pubmed-meshheading:12689549-Oxidoreductases Acting on CH-NH Group Donors,
pubmed-meshheading:12689549-Polymerase Chain Reaction,
pubmed-meshheading:12689549-Polymorphism, Genetic,
pubmed-meshheading:12689549-Spain
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pubmed:year |
2003
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pubmed:articleTitle |
[C677T and A1298C MTHFR polymorphisms in the etiology of neural tube defects in Spanish population].
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pubmed:affiliation |
Sección de Genética. Servicio de Bioquímica Clínica. Hospital Universitario Miguel Servet. Zaragoza. España. joseignaciogutierrez@redfarma.org
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pubmed:publicationType |
Journal Article,
English Abstract
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