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Fig. 1 | BMC Medical Genetics

Fig. 1

From: The identification and characterization of the p.G91 deletion in CRYBA1 in a Chinese family with congenital cataracts

Fig. 1

Overview of CRYBA1 mutation in the family. (a) Pedigree of the two-generation family. Filled symbols indicate individuals affected with CC. In individuals marked with an asterisk, the genotype was determined by exome sequencing. (b) Diagram of the genetic and amino acid sequences of WT and deleted mutant CRYBA1. The “GAG” box is the deleted nucleotide sequence. (c) Results of Sanger sequencing of CRYBA1 from affected and unaffected individuals are presented by chromatogram images

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BMC Medical Genetics

ISSN: 1471-2350

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