Identification of TNFRSF1B as a novel modifier gene in familial combined hyperlipidemia. [electronic resource]
Producer: 20001121Description: 2067-74 p. digitalISSN:- 0964-6906
- Adult
- Alleles
- Apolipoproteins B -- biosynthesis
- Case-Control Studies
- Chromosomes, Human, Pair 1
- DNA Mutational Analysis
- Exons
- Family Health
- Female
- Genetic Linkage
- Genotype
- Haplotypes
- Humans
- Hyperlipidemia, Familial Combined -- blood
- Introns
- Linear Models
- Linkage Disequilibrium
- Male
- Middle Aged
- Phenotype
- Polymorphism, Single Nucleotide
- Receptors, Tumor Necrosis Factor -- blood
- Receptors, Tumor Necrosis Factor, Type II
- Tumor Necrosis Factor-alpha
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Publication Type: Journal Article; Research Support, Non-U.S. Gov't; Research Support, U.S. Gov't, P.H.S.
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