Anderson's disease: Exclusion of apolipoprotein and intracellular lipid transport genes

Arteriosclerosis, Thrombosis, and Vascular Biology

Volumn 19, Issue 10, 1999, Pages 2494-2508

  Dannoura, A Hayssam ^a,b   Berriot Varoqueaux, Nathalie ^b   Amati, Patricia ^b   Abadie, Veronique ^b   Verthier, Nicole ^b   Schmitz, Jacques ^b   Wetterau, John R ^c   Samson Bouma, Marie Elisabeth ^b   Aggerbeck, Lawrence P ^a,d  

^a SORBONNE UNIVERSITÉ   (France)

^b HÔPITAL NECKER ENFANTS MALADES   (France)

^c BRISTOL MYERS SQUIBB   (United States)

^d CNRS   (France)

Author keywords

Anderson's disease; Apolipoprotein B; Chylomicron retention disease; Hypocholesterolemia; Malabsorption

Indexed keywords

APOLIPOPROTEIN; APOLIPOPROTEIN A1; APOLIPOPROTEIN A4; APOLIPOPROTEIN B; APOLIPOPROTEIN C1; APOLIPOPROTEIN C2; APOLIPOPROTEIN C3; APOLIPOPROTEIN E; CHYLOMICRON; FATTY ACID BINDING PROTEIN;

ANDERSON DISEASE; ARTICLE; CHRONIC DIARRHEA; CLINICAL ARTICLE; FAILURE TO THRIVE; FEMALE; GENETIC LINKAGE; HUMAN; HYPERCHOLESTEROLEMIA; HYPOBETALIPOPROTEINEMIA; INFANT; LIPID TRANSPORT; MALABSORPTION; MALE; PATHOGENESIS; PRIORITY JOURNAL; STEATORRHEA; SYNDROME;

EID: 0032871740     PISSN: 10795642     EISSN: None     Source Type: Journal    
DOI: 10.1161/01.ATV.19.10.2494     Document Type: Article

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