Characterisation of severe rod–cone dystrophy in a consanguineous family with a splice site mutation in the MERTK gene | British Journal of Ophthalmology

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Original Article

Characterisation of severe rod–cone dystrophy in a consanguineous family with a splice site mutation in the MERTK gene

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Cite this article as:: Charbel Issa P, Bolz HJ, Ebermann I, et al

Characterisation of severe rod–cone dystrophy in a consanguineous family with a splice site mutation in the MERTK gene

British Journal of Ophthalmology 2009;93:920-925.