Identification of Novel Mutations in Patients with Leber Congenital Amaurosis and Juvenile RP by Genome-wide Homozygosity Mapping with SNP Microarrays
Year: 2007
Type: article
Study design: Observational Study
DOI: 10.1167/iovs.07-0610
Authors: Anneke I. den Hollander, Irma Lopez, Suzanne Yzer, Marijke N. Zonneveld, Irene M. Janssen, Tim M. Strom, Jayne Y. Hehir-Kwa, Joris A. Veltman, Maarten L. Arends, Thomas Meitinger, Maria A. Musarella, L. Ingeborgh van den Born, Gerald A. Fishman, Irene H. Maumenee, Klaus Rohrschneider, Frans P. M. Cremers, Robert K. Koenekoop
Institutions: Radboud University Nijmegen, Radboud University Medical Center, McGill University Health Centre, McGill University, Rotterdam Eye Hospital, Helmholtz Munich, Institut für Humangenetik, Technical University of Munich, State University of New York, University of Illinois Chicago, Johns Hopkins University, Heidelberg University
Language: English
Subfield: Molecular Biology
Domain: Life Sciences
Open Access status: closed
OpenAlex ID: W2071746489