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Frequent occurrence of hypoalphalipoproteinemia due to mutant apolipoprotein A-I gene in the population: a population-based survey.

Authors: Yamakawa-Kobayashi, K  Yanagi, H  Fukayama, H  Hirano, C  Shimakura, Y  Yamamoto, N  Arinami, T  Tsuchiya, S  Hamaguchi, H 
Citation: Yamakawa-Kobayashi K, etal., Hum Mol Genet 1999 Feb;8(2):331-6.
Pubmed: (View Article at PubMed) PMID:9931341

To determine the frequency of familial hypoalphalipoproteinemia in the general population due to mutation of the apolipoprotein A-I (apo A-I) gene, we analyzed sequence variations in the apo A-I gene. The subjects were 67 children with a low high-density lipoprotein (HDL) cholesterol level (


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RGD Object Information
RGD ID: 734583
Created: 2004-02-03
Species: All species
Last Modified: 2004-02-03
Status: ACTIVE


RGD is funded by grant HL64541 from the National Heart, Lung, and Blood Institute on behalf of the NIH.