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Comprehensive registration of DNA sequence variants associated with inherited retinal diseases in Leiden Open Variation Databases.

Cremers, F.P.M., den Dunnen, J.T., Ajmal, M., Hussain, A., Preising, M., Daiger, S.T. and Qamar, R. Human Mutation,Vol: 35, Issue: 1, 147-148 (2014).

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