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. 2020 Nov 13;29(6):897–910. doi: 10.1038/s41431-020-00754-0

Fig. 5. Map of the Arab countries showing the variations with possible founder effects and associated with sporadic and autosomal recessive rod-cone dystrophy.

Fig. 5

Almost all variations with possible founder effects were specific to one country except; (2) c.901C>T; p.(Gln301*) in TULP1 shared in the Kingdom of Saudi Arabia and the Arabian Peninsula, (2) c.2214del; p.(Cys738Trpfs*32) in MERTK shared in the Kingdom of Saudi Arabia and the United Arab Emirates.