NMNAT1 mutations cause Leber congenital amaurosis

Marni J. Falk(Children's Hospital of Philadelphia), Eric A. Pierce(Broad Institute), Eliot L. Berson(Massachusetts Eye and Ear Infirmary), Chitra Kannabiran(L V Prasad Eye Institute), Isabelle Audo(Inserm), Xiaowu Gai(Massachusetts Eye and Ear Infirmary), Eiko Nakamaru‐Ogiso(Johnson Foundation), Christina Chakarova(University College London), Naushin Waseem(UCL Australia), Donna S. Mackay(University of Copenhagen), Zoë Fonseca-Kelly(Massachusetts Eye and Ear Infirmary), Mark Consugar(Massachusetts Eye and Ear Infirmary), Subhadra Jalali(L V Prasad Eye Institute), Rachna Shukla(L V Prasad Eye Institute), Arundhati Dev Borman(Moorfields Eye Hospital), José‐Alain Sahel(University of Pittsburgh), Rui Xiao(National Center on Birth Defects and Developmental Disabilities), Julian Ostrovsky(Children's Hospital of Philadelphia), Christina Zeitz(Centre National de la Recherche Scientifique), Saddek Mohand‐Saïd(Institut de la Vision), Emily Place(MACOM (United States)), Lakshmi Palavalli(L V Prasad Eye Institute), Andrew R. Webster(Moorfields Eye Hospital), Qi Zhang(Chinese Academy of Sciences), Qin Liu(Massachusetts Eye and Ear Infirmary), Shomi S. Bhattacharya(Centro Andaluz de Biología Molecular y Medicina Regenerativa), Magdalena Staniszewska(SDS Optic (Poland)), Anthony T. Moore(Institute of Ophthalmology), Juan C. Perín(Memorial Sloan Kettering Cancer Center)
Nature Genetics
July 29, 2012
Cited by 204


Related Papers