Skip to main content
Figure 2 | BMC Medical Genetics

Figure 2

From: Combinational analysis of linkage and exome sequencing identifies the causative mutation in a Chinese family with congenital cataract

Figure 2

Sequence and pedigree analysis of the C to A transversion in exon 2 of CRYGD . (A) Sequence of the wild-type CRYGD alleles in the unaffected family members. (B) Heterozygous C to A mutation of CRYGD exon 2, resulting in a substitution from proline (P) to threonine (T), was detected in affected patients. A single transversion was observed as a C/A double peak.

Back to article page

BMC Medical Genetics

ISSN: 1471-2350

Contact us