A TULP1 founder mutation, p.Gln301*, underlies a recognisable congenital rod–cone dystrophy phenotype on the Arabian Peninsula | British Journal of Ophthalmology

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Clinical science

A TULP1 founder mutation, p.Gln301*, underlies a recognisable congenital rod–cone dystrophy phenotype on the Arabian Peninsula

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Cite this article as:: Khan AO, Bergmann C, Eisenberger T, et al

A TULP1 founder mutation, p.Gln301*, underlies a recognisable congenital rod–cone dystrophy phenotype on the Arabian Peninsula

British Journal of Ophthalmology 2015;99:488-492.