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Predicate | Object |
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rdf:type | |
lifeskim:mentions | |
pubmed:issue |
5
|
pubmed:dateCreated |
1998-1-30
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pubmed:abstractText |
A linkage and association analysis was made on 14 Italian families with recurrent migraine. We analyzed five chromosomal regions surrounding the candidate genes 5HT1D (1p36.3-34.3), 5HT1B (6q13), 5HT2A (13q14-21), 5HT transporter (17q11.2-12), CACNLB1 (17q11.2-22) and FHM (19p13), using 29 DNA polymorphic markers. All two-point lod scores were negative, and the chi 2 sib-pair analyses were not significant, thus indicating the probable exclusion of these regions as sites of migraine genes in our population.
|
pubmed:language |
eng
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pubmed:journal | |
pubmed:citationSubset |
IM
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pubmed:chemical | |
pubmed:status |
MEDLINE
|
pubmed:month |
Oct
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pubmed:issn |
0392-0461
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pubmed:author | |
pubmed:issnType |
Print
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pubmed:volume |
18
|
pubmed:owner |
NLM
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pubmed:authorsComplete |
Y
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pubmed:pagination |
277-82
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pubmed:dateRevised |
2010-11-18
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pubmed:meshHeading |
pubmed-meshheading:9412851-Chromosome Mapping,
pubmed-meshheading:9412851-DNA,
pubmed-meshheading:9412851-Genetic Linkage,
pubmed-meshheading:9412851-Genome, Human,
pubmed-meshheading:9412851-Humans,
pubmed-meshheading:9412851-Migraine Disorders,
pubmed-meshheading:9412851-Pedigree,
pubmed-meshheading:9412851-Polymorphism, Genetic,
pubmed-meshheading:9412851-Receptors, Serotonin
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pubmed:year |
1997
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pubmed:articleTitle |
Searching for migraine genes: exclusion of 290 cM out of the whole human genome.
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pubmed:affiliation |
Laboratorio di Neurogenetica, Università di Bologna, Italy.
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pubmed:publicationType |
Journal Article,
Research Support, Non-U.S. Gov't
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