Novel human CRYGD rare variant in a Brazilian family with congenital cataract. [electronic resource]

By:

de Figueirêdo, Eugênio Santana

Contributor(s):

Giordano, Gabriel Gorgone
Tavares, Anderson
da Silva, Márcio José
de Vasconcellos, José Paulo Cabral
Arieta, Carlos Eduardo Leite
de Melo, Mônica Barbosa

Producer: 20120110Description: 2207-11 p. digitalISSN:

1090-0535

Subject(s):

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

In: Molecular vision vol. 17

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

APA

de Figueirêdo E. S., Giordano G. G., Tavares A., da Silva M. J., de Vasconcellos J. P. C., Arieta C. E. L. & de Melo M. B. (20120110). Novel human CRYGD rare variant in a Brazilian family with congenital cataract. : Molecular vision.

Chicago

de Figueirêdo Eugênio Santana, Giordano Gabriel Gorgone, Tavares Anderson, da Silva Márcio José, de Vasconcellos José Paulo Cabral, Arieta Carlos Eduardo Leite and de Melo Mônica Barbosa. 20120110. Novel human CRYGD rare variant in a Brazilian family with congenital cataract. : Molecular vision.

Harvard

de Figueirêdo E. S., Giordano G. G., Tavares A., da Silva M. J., de Vasconcellos J. P. C., Arieta C. E. L. and de Melo M. B. (20120110). Novel human CRYGD rare variant in a Brazilian family with congenital cataract. : Molecular vision.

MLA

de Figueirêdo Eugênio Santana, Giordano Gabriel Gorgone, Tavares Anderson, da Silva Márcio José, de Vasconcellos José Paulo Cabral, Arieta Carlos Eduardo Leite and de Melo Mônica Barbosa. Novel human CRYGD rare variant in a Brazilian family with congenital cataract. : Molecular vision. 20120110.

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