Four novel mutations in the RPE65 gene in patients with Leber congenital amaurosis. [electronic resource]
Producer: 20011204Description: 164 p. digitalISSN:- 1098-1004
- Carrier Proteins
- DNA Mutational Analysis
- Exons -- genetics
- Eye Proteins
- Genotype
- Humans
- Introns -- genetics
- Molecular Sequence Data
- Mutation -- genetics
- Optic Atrophy, Hereditary, Leber -- genetics
- Polymorphism, Genetic -- genetics
- Proteins -- genetics
- Retinitis Pigmentosa -- congenital
- cis-trans-Isomerases
No physical items for this record
Publication Type: Journal Article; Research Support, Non-U.S. Gov't; Research Support, U.S. Gov't, P.H.S.
There are no comments on this title.
Log in to your account to post a comment.