Rapid detection of polymorphisms in exons 10, 11 and 12 of the low density lipoprotein receptor gene (LDLR) and their use in a clinical genetic diagnostic setting [1]

Clinical Genetics

Volumn 55, Issue 3, 1999, Pages 212-214

  Heath, K E ^a   Humphries, S E ^a  

^a ROYAL FREE AND UNIVERSITY COLLEGE MEDICAL SCHOOL   (United Kingdom)

Author keywords

[No Author keywords available]

Indexed keywords

DNA; LOW DENSITY LIPOPROTEIN RECEPTOR;

DIAGNOSTIC TEST; DNA POLYMORPHISM; EXON; FAMILIAL HYPERCHOLESTEROLEMIA; GENE FREQUENCY; GENETIC SCREENING; HUMAN; LETTER; NORMAL HUMAN; POLYMERASE CHAIN REACTION; PRIORITY JOURNAL; RECEPTOR GENE; RESTRICTION MAPPING;

AMINO ACID SUBSTITUTION; BASE SEQUENCE; CHILD; DNA; DNA MUTATIONAL ANALYSIS; EXONS; FEMALE; HUMANS; HYPERLIPOPROTEINEMIA TYPE II; MALE; MUTATION; PEDIGREE; POLYMORPHISM, GENETIC; POLYMORPHISM, SINGLE-STRANDED CONFORMATIONAL; RECEPTORS, LDL;

EID: 0032954669     PISSN: 00099163     EISSN: None     Source Type: Journal    
DOI: 10.1034/j.1399-0004.1999.550311.x     Document Type: Letter

References (7)