Fig. 4: Illustration of the AJ founder haplotype relative to the TRPM1 deleted region on chromosome 15. | Human Genome Variation

Fig. 4: Illustration of the AJ founder haplotype relative to the TRPM1 deleted region on chromosome 15.

From: A founder deletion in the TRPM1 gene associated with congenital stationary night blindness and myopia is highly prevalent in Ashkenazi Jews

Fig. 4

The founder haplotype was detected in all TRPM1 deletion carriers. The recombinant founder haplotype was present in most but not all TRPM1 deletion carriers. The founder haplotype is in blue, the TRPM1 deleted region is indicated in red stripes, and the recombinant founder haplotype region is in gray

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