CRB1 mutation spectrum in inherited retinal dystrophies

Human Mutation - Tập 24 Số 5 - Trang 355-369 - 2004
Anneke I. den Hollander1, Jason A. Davis2, Saskia D. van der Velde-Visser1, Marijke N. Zonneveld1, Chiara O. Pierrottet3, Robert K. Koenekoop4, Ulrich Kellner5, L. Ingeborgh van den Born6, John R. Heckenlively7, Carel B. Hoyng8, Penny A. Handford2, Ronald Roepman1, Frans P.M. Cremers1
1Department of Human Genetics, University Medical Center Nijmegen, Nijmegen, The Netherlands
2Molecular and Cellular Biochemistry, Department of Biochemistry, University of Oxford, Oxford, United Kingdom
3Department of Ophthalmology, San Paolo Hospital, University of Milan, Milan, Italy
4Children's Vision Center, McGill University, Montreal, Canada
5Department of Ophthalmology, Charité-Campus Benjamin Franklin, Berlin - Germany
6Rotterdam Eye Hospital, Rotterdam, The Netherlands
7Kellogg Eye Center, University of Michigan, Ann Arbor, Michigan
8Department of Ophthalmology, University Medical Center Nijmegen, Nijmegen, The Netherlands

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Human Mutation

Tập 24 Số 5

355-369

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