TITLE

CHARACTERIZATION OF A NEW LCAT MUTATION CAUSING FAMILIAL LCAT DEFICIENCY (FLD) AND THE ROLE OF APOE AS A MODIFIER GENE OF THE FLD PHENOTYPE

PUB. DATE
December 2009
SOURCE
Clinical & Investigative Medicine;Dec2009 Supplement, Vol. 32, p3
SOURCE TYPE
Academic Journal
DOC. TYPE
Abstract
ABSTRACT
An abstract of the article "Characterization of a New LCAT Mutation Causing Familial LCAT Deficiency (FLD) and the Role of APOE as a Modifier Gene of the FLD Phenotype," by A. Baass, H. Wassef, L. Bernier, R. Dufour, and J. Davignon is presented.
ACCESSION #
47781884

 

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