Detection of two point mutations causing familial defective apolipoprotein B-100 by heteroduplex analysis. [electronic resource]
Producer: 19950503Description: 513-8 p. digitalISSN:- 0890-8508
- Apolipoprotein B-100
- Apolipoproteins B -- deficiency
- Base Sequence
- Coronary Disease -- genetics
- Genes, Dominant -- genetics
- Genetic Carrier Screening
- Humans
- Molecular Sequence Data
- Mutation -- genetics
- Nucleic Acid Heteroduplexes -- isolation & purification
- Pedigree
- Polymerase Chain Reaction -- methods
- Receptors, LDL -- genetics
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Publication Type: Journal Article; Research Support, Non-U.S. Gov't
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