Characterization of a new LCAT mutation causing familial LCAT deficiency (FLD) and the role of APOE as a modifier gene of the FLD phenotype

Author:

Baass Alexis,Wassef Hanny,Tremblay Michel,Bernier Lise,Dufour Robert,Davignon Jean

Publisher

Elsevier BV

Subject

Cardiology and Cardiovascular Medicine

Reference30 articles.

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3. Lecithin cholesterol acyltransferase;Jonas;Biochim Biophys Acta,2000

4. New insights into the regulation of HDL metabolism and reverse cholesterol transport;Lewis;Circulation Res,2005

5. Familial serum-cholesterol esterification failure. A new inborn error of metabolism;Norum;Biochim Biophys Acta,1967

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