Figure 4
From: Deep intronic GPR143 mutation in a Japanese family with ocular albinism
Multiple alignment of the GPR143 intron-5 sequence around the deep cryptic mutation c.659-131âTâ>âG site.
The arrowhead indicates the mutated base. Boxed sequences represent the 41-bp pseudoexon created by the mutation. Asterisks indicate the highly conserved sites among species.
