Survey of familial glaucoma shows a high incidence of cytochrome P450, family 1, subfamily B, polypeptide 1 (CYP1B1) mutations in non-consanguineous congenital forms in a Spanish population. [electronic resource]
Producer: 20130924Description: 1707-22 p. digitalISSN:- 1090-0535
- Anterior Eye Segment -- abnormalities
- Aryl Hydrocarbon Hydroxylases -- genetics
- Consanguinity
- Cytochrome P-450 CYP1B1
- Cytoskeletal Proteins -- genetics
- DNA Mutational Analysis
- Eye Abnormalities -- enzymology
- Eye Diseases, Hereditary
- Eye Proteins -- genetics
- Family
- Female
- Genetic Association Studies
- Genetic Predisposition to Disease
- Glaucoma -- congenital
- Glycoproteins -- genetics
- Health Surveys
- Heterozygote
- Humans
- Incidence
- Male
- Mutation -- genetics
- Pedigree
- Spain -- epidemiology
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Publication Type: Journal Article; Research Support, Non-U.S. Gov't
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