Update of PAX2 mutations in renal coloboma syndrome and establishment of a locus-specific database
Matthew Bower(University of Minnesota), Laurence Heidet(Hôpital Necker-Enfants Malades), Lisa A. Schimmenti(University of Minnesota), Gabriela Peretz‐Amit(Rabin Medical Center), Laura Martin(University of Rochester Medical Center), Judith Allanson(Addenbrooke's Hospital), Gerard C. P. Schaafsma(Leiden University Medical Center), Gil Binenbaum(Children's Hospital of Philadelphia), Abhay Vats(University of Pittsburgh), Sujatha Sastry(Children's Hospital of Michigan), Luisa Murer(University of Padua), Robert Gise(Children's Medical Center), Richard G. Weleber(Oregon Health & Science University), Joanne Dixon(Wellington Hospital), David Mowat(UNSW Sydney), John A. Sayer(Newcastle University), Vincent Morinière(Hôpital Necker-Enfants Malades), Francesco Benedicenti(Ospedale di Bolzano), Pierre Cochat(Société Nationale des Chemins de Fer Français (France)), Rémi Salomon(Inserm), Dina J. Zand(Children's National), Elisa Benetti, Carolyn Wilson-Brackett, Eric A. Pierce(Broad Institute), Marni J. Falk(Children's Hospital of Philadelphia), Berta Warman(Minnesota State Colleges and Universities System), Tadashi Sato(Juntendo University), Wen‐Hann Tan(Boston Children's Hospital), Holly Feret(Children's Hospital of Philadelphia), Susan M. White(The University of Melbourne), Xinjing Wang(Shanghai Jiao Tong University), Romano Tenconi(University of Padua), Corinne Antignac(Hôpital Necker-Enfants Malades), Stéphane Decramer(Inserm), David W. Stockton(Baylor College of Medicine), Emily Place(MACOM (United States)), Ann E. Salerno(Harvard University), Uffe Birk Jensen(Aarhus University Hospital), Kisha Johnson(Rush University Medical Center), Michael R. Eccles(Dunedin Public Hospital), Rajiv Kumar(Auckland City Hospital), Lawrence R. Shoemaker(Kosair Children's Hospital), Régen Drouin(Université de Sherbrooke), Alasdair G. W. Hunter(Children's Hospital of Eastern Ontario), Marie Pierre Lavocat(Hôpital Nord), Nancy Rodig(Unknown), Hiep T. Nguyen, Philippe Vanhille(Centre Hospitalier de Valenciennes)
Cited by 158
Related Papers
Safety and Efficacy of Gene Transfer for Leber's Congenital Amaurosis
|New England Journal of Medicine|2008|2.1k
Tuberous Sclerosis Complex Diagnostic Criteria Update: Recommendations of the 2012 International Tuberous Sclerosis Complex Consensus Conference
|Pediatric Neurology|2013|1.5k
Suppression of retinal neovascularization in vivo by inhibition of vascular endothelial growth factor (VEGF) using soluble VEGF-receptor chimeric proteins.
|Proceedings of the National Academy of Sciences|1995|1.3k
Vascular endothelial growth factor/vascular permeability factor expression in a mouse model of retinal neovascularization.
|Proceedings of the National Academy of Sciences|1995|1k