Source:http://linkedlifedata.com/resource/pubmed/id/12372939
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Predicate | Object |
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rdf:type | |
lifeskim:mentions | |
pubmed:issue |
3
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pubmed:dateCreated |
2002-10-9
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pubmed:abstractText |
Familial juvenile gouty nephropathy (FJGN, MIM 162000) is an autosomal-dominant renal disease characterized by underexcretion-type hyperuricemia, gouty arthritis, and progressive renal disease at younger ages. We analyzed the localization of the responsible gene for FJGN concerning the chromosomal region of 16p12 using parametric linkage analysis in our FJGN.
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pubmed:language |
eng
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pubmed:journal | |
pubmed:citationSubset |
IM
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pubmed:status |
MEDLINE
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pubmed:issn |
0028-2766
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pubmed:author | |
pubmed:copyrightInfo |
Copyright 2002 S. Karger AG, Basel
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pubmed:issnType |
Print
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pubmed:volume |
92
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pubmed:owner |
NLM
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pubmed:authorsComplete |
Y
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pubmed:pagination |
573-5
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pubmed:dateRevised |
2010-11-18
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pubmed:meshHeading |
pubmed-meshheading:12372939-Child,
pubmed-meshheading:12372939-Family Health,
pubmed-meshheading:12372939-Female,
pubmed-meshheading:12372939-Gout,
pubmed-meshheading:12372939-Humans,
pubmed-meshheading:12372939-Hyperuricemia,
pubmed-meshheading:12372939-Lod Score,
pubmed-meshheading:12372939-Male,
pubmed-meshheading:12372939-Pedigree,
pubmed-meshheading:12372939-Renal Insufficiency
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pubmed:year |
2002
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pubmed:articleTitle |
Familial juvenile gouty nephropathy: exclusion of 16p12 from the candidate locus.
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pubmed:affiliation |
Division of Kidney and Hypertension, Department of Internal Medicine, Jikei University School of Medicine, Tokyo, Japan. i-ohno@jikei.ac.jp
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pubmed:publicationType |
Journal Article,
Research Support, Non-U.S. Gov't
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