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The Human apM-1, an Adipocyte-Specific Gene Linked to the Family of TNF's and to Genes Expressed in Activated T Cells, Is Mapped to Chromosome 1q21.3-q23, a Susceptibility Locus Identified for Familial Combined Hyperlipidaemia (FCH)

Metabolic SyndromeActivated T CellsHuman Apm-1Genetic DeterminantMetabolic DisorderGenetic DisorderFamilial Combined HyperlipidaemiaGeneticsInherited Metabolic DiseaseGenetic EpidemiologyHuman PolymorphismPathologyMolecular GeneticsMedicine