A 129-kb deletion on chromosome 12 confers substantial protection against rheumatoid arthritis, implicating the gene SLC2A3.
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Copy-number variation of the neuronal glucose transporter gene SLC2A3 and age of onset in Huntington's disease.Copy-Number Variation of the Glucose Transporter Gene SLC2A3 and Congenital Heart Defects in the 22q11.2 Deletion Syndrome.Analysis of Copy Number Variation Using the Paralogue Ratio Test (PRT).SRBreak: A Read-Depth and Split-Read Framework to Identify Breakpoints of Different Events Inside Simple Copy-Number Variable Regions.The SLC2A14 gene, encoding the novel glucose/dehydroascorbate transporter GLUT14, is associated with inflammatory bowel disease.The SLC2A14 gene: genomic locus, tissue expression, splice variants, and subcellular localization of the protein.Autosomal and X chromosome structural variants are associated with congenital heart defects in Turner syndrome: The NHLBI GenTAC registry.
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A 129-kb deletion on chromosome 12 confers substantial protection against rheumatoid arthritis, implicating the gene SLC2A3.
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article científic
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article scientifique
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articolo scientifico
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artigo científico
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bilimsel makale
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scientific article published on 02 December 2013
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vedecký článok
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vetenskaplig artikel
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A 129-kb deletion on chromosom ...... , implicating the gene SLC2A3.
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A 129-kb deletion on chromosom ...... , implicating the gene SLC2A3.
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A 129-kb deletion on chromosom ...... , implicating the gene SLC2A3.
@en
A 129-kb deletion on chromosom ...... , implicating the gene SLC2A3.
@nl
prefLabel
A 129-kb deletion on chromosom ...... , implicating the gene SLC2A3.
@en
A 129-kb deletion on chromosom ...... , implicating the gene SLC2A3.
@nl
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A 129-kb deletion on chromosom ...... s, implicating the gene SLC2A3
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Anthony J Brookes
Johnny C Lorentzen
Katherine E Reekie
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10.1002/HUMU.22471
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2013-12-02T00:00:00Z