Novel mutations in RPE65 identified in consanguineous Pakistani families with retinal dystrophy. [electronic resource]
Producer: 20130924Description: 1554-64 p. digitalISSN:- 1090-0535
- Amino Acid Sequence
- Base Sequence
- Chromosomes, Human, Pair 1 -- genetics
- Consanguinity
- Conserved Sequence -- genetics
- DNA Mutational Analysis
- Electroretinography
- Family
- Female
- Fundus Oculi
- Genetic Predisposition to Disease
- Haplotypes -- genetics
- Humans
- Lod Score
- Male
- Molecular Sequence Data
- Mutation -- genetics
- Pakistan
- Pedigree
- Retinal Dystrophies -- genetics
- cis-trans-Isomerases -- chemistry
No physical items for this record
Publication Type: Journal Article; Research Support, Non-U.S. Gov't
There are no comments on this title.
Log in to your account to post a comment.