11p13 deletions can be more frequent than the PAX6 gene point mutations in Polish patients with aniridia. [electronic resource]
Producer: 20140114Description: 345-51 p. digitalISSN:- 2190-3883
- Aniridia -- ethnology
- Base Sequence
- Chromosome Deletion
- Chromosomes, Human, Pair 11
- DNA Primers -- genetics
- Exons
- Eye Proteins -- genetics
- Gene Deletion
- Genomics
- Heterozygote
- Homeodomain Proteins -- genetics
- Humans
- Introns
- Molecular Sequence Data
- Mutation
- PAX6 Transcription Factor
- Paired Box Transcription Factors -- genetics
- Phenotype
- Point Mutation
- Poland
- Repressor Proteins -- genetics
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Publication Type: Journal Article
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