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rdf:type |
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lifeskim:mentions |
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pubmed:issue |
23
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pubmed:dateCreated |
2009-6-9
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pubmed:abstractText |
We assessed the hypotheses that non-major histocompatibility complex multiple sclerosis (MS) susceptibility loci would be common to sporadic cases and multiplex families, that they would have larger effects in multiplex families, and that the aggregation of susceptibility loci contributes to the increased prevalence of MS in such families.
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pubmed:language |
eng
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pubmed:journal |
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pubmed:citationSubset |
AIM
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pubmed:chemical |
http://linkedlifedata.com/resource/pubmed/chemical/Antigens, CD58,
http://linkedlifedata.com/resource/pubmed/chemical/CLEC16A protein, human,
http://linkedlifedata.com/resource/pubmed/chemical/EVI5 protein, human,
http://linkedlifedata.com/resource/pubmed/chemical/Histocompatibility Antigens,
http://linkedlifedata.com/resource/pubmed/chemical/IL2RA protein, human,
http://linkedlifedata.com/resource/pubmed/chemical/Interleukin-2 Receptor alpha Subunit,
http://linkedlifedata.com/resource/pubmed/chemical/Lectins, C-Type,
http://linkedlifedata.com/resource/pubmed/chemical/Monosaccharide Transport Proteins,
http://linkedlifedata.com/resource/pubmed/chemical/Nuclear Proteins,
http://linkedlifedata.com/resource/pubmed/chemical/Receptors, Interleukin-7
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pubmed:status |
MEDLINE
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pubmed:month |
Jun
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pubmed:issn |
1526-632X
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pubmed:author |
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pubmed:issnType |
Electronic
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pubmed:day |
9
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pubmed:volume |
72
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pubmed:owner |
NLM
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pubmed:authorsComplete |
Y
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pubmed:pagination |
1984-8
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pubmed:dateRevised |
2010-5-20
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pubmed:meshHeading |
pubmed-meshheading:19506219-Alleles,
pubmed-meshheading:19506219-Antigens, CD58,
pubmed-meshheading:19506219-Case-Control Studies,
pubmed-meshheading:19506219-Chromosome Mapping,
pubmed-meshheading:19506219-DNA Mutational Analysis,
pubmed-meshheading:19506219-Family,
pubmed-meshheading:19506219-Female,
pubmed-meshheading:19506219-Gene Frequency,
pubmed-meshheading:19506219-Genetic Predisposition to Disease,
pubmed-meshheading:19506219-Genetic Testing,
pubmed-meshheading:19506219-Genetic Variation,
pubmed-meshheading:19506219-Genome-Wide Association Study,
pubmed-meshheading:19506219-Genotype,
pubmed-meshheading:19506219-Histocompatibility Antigens,
pubmed-meshheading:19506219-Humans,
pubmed-meshheading:19506219-Interleukin-2 Receptor alpha Subunit,
pubmed-meshheading:19506219-Lectins, C-Type,
pubmed-meshheading:19506219-Linkage Disequilibrium,
pubmed-meshheading:19506219-Male,
pubmed-meshheading:19506219-Molecular Epidemiology,
pubmed-meshheading:19506219-Monosaccharide Transport Proteins,
pubmed-meshheading:19506219-Multiple Sclerosis,
pubmed-meshheading:19506219-Nuclear Proteins,
pubmed-meshheading:19506219-Pedigree,
pubmed-meshheading:19506219-Polymorphism, Single Nucleotide,
pubmed-meshheading:19506219-Prevalence,
pubmed-meshheading:19506219-Receptors, Interleukin-7,
pubmed-meshheading:19506219-Risk Factors
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pubmed:year |
2009
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pubmed:articleTitle |
Risk alleles for multiple sclerosis in multiplex families.
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pubmed:affiliation |
Wellcome Trust Centre for Human Genetics, Department of Clinical Neurology, University of Oxford, UK.
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pubmed:publicationType |
Journal Article,
Research Support, Non-U.S. Gov't
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