Familial defective apolipoprotein B-100: A mutation of apolipoprotein B that causes hypercholesterolemia

Journal of Lipid Research

Volumn 31, Issue 8, 1990, Pages 1337-1349

  Innerarity, T L ^a   Mahley, R W ^a   Weisgraber, K H ^a   Bersot, T P ^a   Krauss, R M ^a   Vega, G L ^a   Grundy, S M ^a   Friedl, W ^a   Davignon, J ^a   McCarthy, B J ^a  

^a GLADSTONE INSTITUTES   (United States)

Author keywords

Atherosclerosis; Cholesterol; Genetic mutation; LDL; LDL receptor; Review

Indexed keywords

APOLIPOPROTEIN B100; LOW DENSITY LIPOPROTEIN; RECEPTOR;

CASE REPORT; HUMAN; HYPERCHOLESTEROLEMIA; MUTATION; PRIORITY JOURNAL; REVIEW;

APOLIPOPROTEINS B; FEMALE; GENES; HUMAN; HYPERCHOLESTEROLEMIA, FAMILIAL; MALE; MUTATION; PEDIGREE; RESTRICTION MAPPING; SUPPORT, U.S. GOV'T, P.H.S.;

EID: 0025102741     PISSN: 00222275     EISSN: None     Source Type: Journal    
DOI: None     Document Type: Review

References (0)