Familial defective apolipoprotein B and familial hypobetalipoproteinemia in one family: Two neutralizing mutations

Annals of Internal Medicine

Volumn 148, Issue 9, 2008, Pages 712-714

  Van Der Graaf, Anouk ^a   Fouchier, Sigrid W ^a   Vissers, Maud N ^a   Defesche, Joep C ^a   Wiegman, Albert ^a   Sankatsing, Raaj R ^a   Hutten, Barbara A ^a   Trip, Mieke D ^a   Kastelein, John J P ^a  

^a UNIVERSITY OF AMSTERDAM   (Netherlands)

Author keywords

[No Author keywords available]

Indexed keywords

APOLIPOPROTEIN B; LOW DENSITY LIPOPROTEIN CHOLESTEROL;

CASE REPORT; CHILD; CHOLESTEROL BLOOD LEVEL; CORONARY ARTERY DISEASE; FAMILIAL DISEASE; FEMALE; GENE MUTATION; HUMAN; HYPERCHOLESTEROLEMIA; HYPOBETALIPOPROTEINEMIA; HYPOCHOLESTEROLEMIA; LETTER; LIPOPROTEIN METABOLISM; MALE; PRIORITY JOURNAL;

EID: 43449136801     PISSN: 00034819     EISSN: None     Source Type: Journal    
DOI: 10.7326/0003-4819-148-9-200805060-00022     Document Type: Letter

References (5)