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OFD1 Is Mutated in X-Linked Joubert Syndrome and Interacts with LCA5-Encoded Lebercilin Karlien L.M. Coene, Ronald Roepman, Dan Doherty, Bushra Afroze, Hester Y. Kroes, Stef J.F. Letteboer, Lock H. Ngu, Bartlomiej Budny, Erwin van Wijk, Nicholas T. Gorden, Malika Azhimi, Christel Thauvin-Robinet, Joris A. Veltman, Mireille Boink, Tjitske Kleefstra, Frans P.M. Cremers, Hans van Bokhoven, Arjan P.M. de Brouwer The American Journal of Human Genetics Volume 85, Issue 4, Pages (October 2009) DOI: /j.ajhg Copyright © 2009 The American Society of Human Genetics Terms and Conditions Terms and Conditions
Figure 1 The American Journal of Human Genetics , DOI: ( /j.ajhg ) Copyright © 2009 The American Society of Human Genetics Terms and Conditions Terms and Conditions
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Figure 3 The American Journal of Human Genetics , DOI: ( /j.ajhg ) Copyright © 2009 The American Society of Human Genetics Terms and Conditions Terms and Conditions
Figure 4 The American Journal of Human Genetics , DOI: ( /j.ajhg ) Copyright © 2009 The American Society of Human Genetics Terms and Conditions Terms and Conditions
Figure 5 The American Journal of Human Genetics , DOI: ( /j.ajhg ) Copyright © 2009 The American Society of Human Genetics Terms and Conditions Terms and Conditions
Figure 6 The American Journal of Human Genetics , DOI: ( /j.ajhg ) Copyright © 2009 The American Society of Human Genetics Terms and Conditions Terms and Conditions
Figure 7 The American Journal of Human Genetics , DOI: ( /j.ajhg ) Copyright © 2009 The American Society of Human Genetics Terms and Conditions Terms and Conditions
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