A rare penetrant mutation in CFH confers high risk of age-related macular degeneration. [electronic resource]
Producer: 20120120Description: 1232-6 p. digitalISSN:- 1546-1718
- Aged
- Aged, 80 and over
- Case-Control Studies
- Complement Factor H -- genetics
- Female
- Genetic Predisposition to Disease
- Haplotypes
- Heterozygote
- High-Throughput Nucleotide Sequencing
- Humans
- Linkage Disequilibrium
- Macular Degeneration -- genetics
- Male
- Middle Aged
- Mutation, Missense
- Penetrance
- Polymorphism, Single Nucleotide
- Principal Component Analysis
- Risk Factors
- Sequence Analysis, DNA
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Publication Type: Journal Article; Research Support, N.I.H., Extramural; Research Support, Non-U.S. Gov't
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