Alu-element insertion in an OPA1 intron sequence associated with autosomal dominant optic atrophy. [electronic resource]
Producer: 20100310Description: 178-83 p. digitalISSN:- 1090-0535
- Adolescent
- Adult
- Alu Elements -- genetics
- Base Sequence
- Child
- DNA Mutational Analysis
- Family
- Female
- GTP Phosphohydrolases -- genetics
- Genetic Predisposition to Disease
- Humans
- Introns -- genetics
- Male
- Middle Aged
- Molecular Sequence Data
- Mutagenesis, Insertional -- genetics
- Optic Atrophy, Autosomal Dominant -- genetics
- Pedigree
- Young Adult
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Publication Type: Journal Article; Research Support, Non-U.S. Gov't
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