Human ATP-binding cassette transporter 1 (ABC1): Genomic organization and identification of the genetic defect in the original Tangier disease kindred

Tangier disease is characterized by low serum high density lipoproteins and a biochemical defect in the cellular efflux of lipids to high density lipoproteins. ABC1, a member of the ATP-binding cassette family, recently has been identified as the defective gene in Tangier disease. We report here the...

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Detaylı Bibliyografya
Asıl Yazarlar: Remaley, Alan T., Rust, Stephan, Rosier, Marie, Knapper, Cathy, Naudin, Laurent, Broccardo, Cyril, Peterson, Katherine M., Koch, Christine, Arnould, Isabelle, Prades, Catherine, Duverger, Nicholas, Funke, Harald, Assman, Gerd, Dinger, Maria, Dean, Michael, Chimini, Giovanna, Santamarina-Fojo, Silvia, Fredrickson, Donald S., Denefle, Patrice, Brewer, H. Bryan
Materyal Türü: Artigo
Dil:Inglês
Baskı/Yayın Bilgisi: The National Academy of Sciences 1999
Konular:
Biological Sciences
Online Erişim:https://ncbi.nlm.nih.gov/pmc/articles/PMC23050/
https://ncbi.nlm.nih.gov/pubmed/10535983
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