TY  - GEN
AU  - Kotze,M J
AU  - Langenhoven,E
AU  - Peeters,A V
AU  - Theart,L
AU  - Oosthuizen,C J
TI  - Detection of two point mutations causing familial defective apolipoprotein B-100 by heteroduplex analysis
SN  - 0890-8508
PY  - 1995///0503
KW  - Apolipoprotein B-100
KW  - Apolipoproteins B
KW  - deficiency
KW  - Base Sequence
KW  - Coronary Disease
KW  - genetics
KW  - Genes, Dominant
KW  - Genetic Carrier Screening
KW  - Humans
KW  - Molecular Sequence Data
KW  - Mutation
KW  - Nucleic Acid Heteroduplexes
KW  - isolation & purification
KW  - Pedigree
KW  - Polymerase Chain Reaction
KW  - methods
KW  - Receptors, LDL
N1  - Publication Type: Journal Article; Research Support, Non-U.S. Gov't
UR  - https://doi.org/10.1006/mcpr.1994.1072
ER  -