Structural assessment of PITX2, FOXC1, CYP1B1, and GJA1 genes in patients with Axenfeld-Rieger syndrome with developmental glaucoma. [electronic resource]
Producer: 20060606Description: 1803-9 p. digitalISSN:- 0146-0404
- Adolescent
- Adult
- Anterior Eye Segment -- abnormalities
- Aryl Hydrocarbon Hydroxylases
- Child
- Connexin 43 -- genetics
- Cytochrome P-450 CYP1B1
- Cytochrome P-450 Enzyme System -- genetics
- DNA Mutational Analysis
- Eye Abnormalities -- genetics
- Female
- Forkhead Transcription Factors -- genetics
- Glaucoma -- genetics
- Homeodomain Proteins -- genetics
- Humans
- Male
- Mutation
- Pedigree
- Polymerase Chain Reaction
- Polymorphism, Single Nucleotide
- Syndrome
- Transcription Factors -- genetics
- Homeobox Protein PITX2
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Publication Type: Journal Article; Research Support, Non-U.S. Gov't
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