Neonatal diagnosis of familial hypercholesterolemia in newborns born to a parent with a molecularly defined heterozygous familial hypercholesterolemia

Arteriosclerosis, Thrombosis, and Vascular Biology

Volumn 17, Issue 11, 1997, Pages 3332-3337

  Vuorio, A F ^a   Turtola, H ^a   Kontula, K ^a  

^a UNIVERSITY OF HELSINKI   (Finland)

Author keywords

Cord blood; Low density lipoprotein; Mutation; North Karelia; Polymerase chain reaction; Receptors

Indexed keywords

LIPID; LOW DENSITY LIPOPROTEIN CHOLESTEROL; LOW DENSITY LIPOPROTEIN RECEPTOR;

ARTICLE; CHOLESTEROL BLOOD LEVEL; CLINICAL ARTICLE; FAMILIAL HYPERCHOLESTEROLEMIA; FEMALE; GENE MUTATION; HETEROZYGOSITY; HUMAN; LIPID ANALYSIS; LIPID BLOOD LEVEL; MALE; NEWBORN; PHENOTYPE; POLYMERASE CHAIN REACTION; PRIORITY JOURNAL; UMBILICAL CORD BLOOD;

EID: 0031439541     PISSN: 10795642     EISSN: None     Source Type: Journal    
DOI: 10.1161/01.ATV.17.11.3332     Document Type: Article

References (42)