Mutations in the CEP290 (NPHP6) Gene Are a Frequent Cause of Leber Congenital Amaurosis
Anneke I. den Hollander(Radboud University Nijmegen), Robert K. Koenekoop(McGill University Health Centre), Suzanne Yzer(Radboud University Nijmegen), Irma López(McGill University Health Centre), Maarten Arends(Radboud University Nijmegen), Krysta Voesenek(Radboud University Nijmegen), Marijke N. Zonneveld(Radboud University Nijmegen), Tim M. Strom(Institute of Human Genetics), Thomas Meitinger(Institute of Human Genetics), Han G. Brunner(Radboud University Nijmegen), Carel B. Hoyng(Radboud University Nijmegen), L. Ingeborgh van den Born(Rotterdam Eye Hospital), Klaus Rohrschneider(Heidelberg University), Frans P.M. Cremers(Radboud University Nijmegen)
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