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. 2013 Nov 6;3(11):e004030. doi: 10.1136/bmjopen-2013-004030

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Published by the BMJ Publishing Group Limited. For permission to use (where not already granted under a licence) please go to http://group.bmj.com/group/rights-licensing/permissions

This is an Open Access article distributed in accordance with the Creative Commons Attribution Non Commercial (CC BY-NC 3.0) license, which permits others to distribute, remix, adapt, build upon this work non-commercially, and license their derivative works on different terms, provided the original work is properly cited and the use is non-commercial. See: http://creativecommons.org/licenses/by-nc/3.0/

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Fundus photographs of two probands with mutations in the PRPF31 gene. (A, B) Proband IV14 is from family autosomal dominant retinitis pigmentosa (adRP)-19. (C, D) Proband III9 is from family adRP-61. Typical RP changes can be seen.