Human genes involved in lipolysis of plasma lipoproteins: Mapping of loci for lipoprotein lipase to 8p22 and hepatic lipase to 15q21

Author:

Sparkes Robert S.,Zollman Susan,Klisak Ivana,Kirchgessner Todd G.,Komaromy Michael C.,Mohandas T.,Schotz Michael C.,Lusis Aldons J.

Publisher

Elsevier BV

Subject

Genetics

Reference19 articles.

1. The structural gene for human lecithin: cholesterol acyl transferase (LCAT) maps to 16q22;Azoulay;Cytogenet. Cell Genet,1986

2. Lipoprotein abnormalities associated with a familial deficiency of hepatic lipase;Breckenridge;Atherosclerosis,1982

3. Primary lipoprotein lipase deficiency;Brunzell;Adv. Exp. Med. Biol,1986

4. An improved method for G banding chromosomes after in situ hybridization;Cannizzaro;Cytogenet. Cell Genet,1984

5. Deficiency of hepatic lipase activity in post-heparin plasma in familial hyper-α-triglyceridemia;Carlson;Acta Med. Scand,1986

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