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Fig. 3 | BMC Ophthalmology

Fig. 3

From: A novel homozygous missense substitution p.Thr313Ile in the PDE6B gene underlies autosomal recessive retinitis pigmentosa in a consanguineous Pakistani family

Fig. 3

Homozygosity mapping showing genome-wide autozygous interval as vertical blue peaks along all the autosomes (1–22 chromosomes) shown on horizontal axis. The red arrow indicates an autozygous interval (~ 2.36 Mb) harboring PDE6B gene in which mutation was uncovered. Total autozygosity (293.14 Mb) is shown on top of the figure

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BMC Ophthalmology

ISSN: 1471-2415

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