Novel human CRYGD rare variant in a Brazilian family with congenital cataract.

de Figueirêdo, Eugênio Santana

Novel human CRYGD rare variant in a Brazilian family with congenital cataract. [electronic resource] - Molecular vision 2011 - 2207-11 p. digital

Publication Type: Journal Article

1090-0535


Adult
Base Sequence
Brazil
Case-Control Studies
Cataract--congenital
Crystallins--genetics
DNA Mutational Analysis
Family
Female
Genotype
Heterozygote
Humans
Infant, Newborn
Male
Molecular Sequence Data
Mutation, Missense
Pedigree
Phenotype
Polymerase Chain Reaction
Sequence Alignment
gamma-Crystallins--genetics