A novel founder BBS1 mutation explains a unique high prevalence of Bardet–Biedl syndrome in the Faroe Islands | British Journal of Ophthalmology

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Original Article

A novel founder BBS1 mutation explains a unique high prevalence of Bardet–Biedl syndrome in the Faroe Islands

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Cite this article as:: Hjortshøj TD, Grønskov K, Brøndum-Nielsen K, et al

A novel founder BBS1 mutation explains a unique high prevalence of Bardet–Biedl syndrome in the Faroe Islands

British Journal of Ophthalmology 2009;93:409-413.