Skip to main content
Fig. 4 | BMC Medical Genetics

Fig. 4

From: Novel mutations identified in Chinese families with autosomal dominant congenital cataracts by targeted next-generation sequencing

Fig. 4

The multiple-sequence alignments from different vertebrate species. (a-d) The amino acid alterations, F52 L of GJA8 in Family 1, T511 M of EPHA2 in Family 4 and R119H of HSF4 in Family 5 were located in highly conserved region among all vertebrate species and were marked with box. While G602R of BFSP1 in Family 3 had lower conservative propertys

Back to article page