Autosomal recessive congenital cataract in consanguineous Pakistani families is associated with mutations in GALK1. [electronic resource]
Producer: 20100511Description: 682-8 p. digitalISSN:- 1090-0535
- Amino Acid Sequence
- Base Sequence
- Cataract -- congenital
- Consanguinity
- DNA Mutational Analysis
- Family
- Female
- Galactokinase -- chemistry
- Genes, Recessive -- genetics
- Genetic Predisposition to Disease
- Humans
- Lod Score
- Male
- Molecular Sequence Data
- Mutation -- genetics
- Pakistan
- Pedigree
- Sequence Alignment
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.