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

Authors

  1. Dr T D Hjortshøj, Kennedy Center, Gl. Landevej 7, DK-2600 Glostrup, Denmark; tid{at}kennedy.dk
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Citation

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.

Publication history

  • Accepted May 31, 2008
  • First published July 31, 2008.
Online issue publication 
March 22, 2016

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2009 BMJ Publishing Group