MedPed FH: A paradigm for other common monogenic diseases in South Africa

Atherosclerosis

Volumn 144, Issue 2, 1999, Pages 467-468

  Kotze, M J ^a   Callis, M ^a   Stephenson, S H ^a  

^a UNIVERSITY OF UTAH SCHOOL OF MEDICINE   (United States)

Author keywords

[No Author keywords available]

Indexed keywords

LOW DENSITY LIPOPROTEIN RECEPTOR;

ARTICLE; AUTOSOMAL DOMINANT INHERITANCE; FAMILIAL HYPERCHOLESTEROLEMIA; GENE MUTATION; GENETIC SCREENING; GENOTYPE; HEMOCHROMATOSIS; HUMAN; PRIORITY JOURNAL; SOUTH AFRICA;

CHILD; CHROMOSOME ABERRATIONS; CHROMOSOME DISORDERS; GENES, DOMINANT; GENETICS, POPULATION; HETEROZYGOTE DETECTION; HUMANS; HYPERLIPOPROTEINEMIA TYPE II; MUTATION; RECEPTORS, LDL; SOUTH AFRICA;

EID: 0032977827     PISSN: 00219150     EISSN: None     Source Type: Journal    
DOI: 10.1016/S0021-9150(99)00096-9     Document Type: Article

References (0)