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rdf:type |
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lifeskim:mentions |
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pubmed:issue |
9
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pubmed:dateCreated |
2005-9-5
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pubmed:databankReference |
http://linkedlifedata.com/resource/pubmed/xref/GENBANK/AC068631,
http://linkedlifedata.com/resource/pubmed/xref/OMIM/121015,
http://linkedlifedata.com/resource/pubmed/xref/OMIM/123580,
http://linkedlifedata.com/resource/pubmed/xref/OMIM/123590,
http://linkedlifedata.com/resource/pubmed/xref/OMIM/123610,
http://linkedlifedata.com/resource/pubmed/xref/OMIM/123620,
http://linkedlifedata.com/resource/pubmed/xref/OMIM/123680,
http://linkedlifedata.com/resource/pubmed/xref/OMIM/123690,
http://linkedlifedata.com/resource/pubmed/xref/OMIM/154045,
http://linkedlifedata.com/resource/pubmed/xref/OMIM/154050,
http://linkedlifedata.com/resource/pubmed/xref/OMIM/600429,
http://linkedlifedata.com/resource/pubmed/xref/OMIM/600897,
http://linkedlifedata.com/resource/pubmed/xref/OMIM/600929,
http://linkedlifedata.com/resource/pubmed/xref/OMIM/602438,
http://linkedlifedata.com/resource/pubmed/xref/OMIM/603212,
http://linkedlifedata.com/resource/pubmed/xref/RefSeq/NP_060011
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pubmed:abstractText |
Congenital or childhood cataract is clinically and genetically a highly heterogeneous lens disorder in children. Autosomal dominant inheritance is most common.
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pubmed:language |
eng
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pubmed:journal |
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pubmed:citationSubset |
IM
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pubmed:chemical |
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pubmed:status |
MEDLINE
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pubmed:month |
Sep
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pubmed:issn |
1468-6244
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pubmed:author |
pubmed-author:DingXX,
pubmed-author:GaySS,
pubmed-author:LULL,
pubmed-author:LUMM,
pubmed-author:LinKK,
pubmed-author:LuGG,
pubmed-author:LuJJ,
pubmed-author:MASS,
pubmed-author:ShenYY,
pubmed-author:SuhBB,
pubmed-author:TankTT
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pubmed:issnType |
Electronic
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pubmed:volume |
42
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pubmed:owner |
NLM
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pubmed:authorsComplete |
Y
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pubmed:pagination |
706-10
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pubmed:dateRevised |
2008-11-20
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pubmed:meshHeading |
pubmed-meshheading:16141006-Amino Acid Sequence,
pubmed-meshheading:16141006-Animals,
pubmed-meshheading:16141006-Base Sequence,
pubmed-meshheading:16141006-Cataract,
pubmed-meshheading:16141006-China,
pubmed-meshheading:16141006-DNA Mutational Analysis,
pubmed-meshheading:16141006-Family,
pubmed-meshheading:16141006-Genes, Dominant,
pubmed-meshheading:16141006-Haplotypes,
pubmed-meshheading:16141006-Humans,
pubmed-meshheading:16141006-Lod Score,
pubmed-meshheading:16141006-Molecular Sequence Data,
pubmed-meshheading:16141006-Mutation,
pubmed-meshheading:16141006-Pedigree,
pubmed-meshheading:16141006-Sequence Alignment,
pubmed-meshheading:16141006-gamma-Crystallins
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pubmed:year |
2005
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pubmed:articleTitle |
Gamma-S crystallin gene (CRYGS) mutation causes dominant progressive cortical cataract in humans.
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pubmed:affiliation |
Eye Centre of Tianjin Medical University, Tianjin, China.
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pubmed:publicationType |
Journal Article,
Research Support, Non-U.S. Gov't
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