Screening of a Large Cohort of Leber Congenital Amaurosis and Retinitis Pigmentosa Patients Identifies Novel LCA5 Mutations and New Genotype–Phenotype Correlations. Issue 1 (30th October 2013)

• Record Type: Journal Article
• Authors: Mackay, Donna S.; Borman, Arundhati Dev; Sui, Ruifang; van den, L. Ingeborgh; Berson, Eliot L.; Ocaka, Louise A.; Davidson, Alice E.; Heckenlively, John R.; Branham, Kari; Ren, Huanan; Lopez, Irma; Maria, Maleeha; Azam, Maleeha; Henkes, Arjen; Blokland, Ellen; Andreasson, [Sten; de, Elfride; Bennett, Jean; Chader, Gerald J.; Berger, Wolfgang; Golovleva, Irina; Greenberg, Jacquie; den Hollander, Anneke I.; Klaver, Caroline C.W.; Klevering, B. Jeroen; Lorenz, Birgit; Preising, Markus N.; Ramesar, Raj; Roberts, Lisa; Roepman, Ronald; Rohrschneider, Klaus; Wissinger], Bernd; Qamar, Raheel; Webster, Andrew R.; Cremers, Frans P.M.; Moore, Anthony T.; Koenekoop, Robert K.;
• Is Part Of: Human mutation. Volume 35:Issue 1(2014:Jan.)
• Page Start: 150
• Page End: 150
• Publication Date: 2013-10-30
• Subjects: Human chromosome abnormalities -- Periodicals; Mutation (Biology) -- Periodicals; 616.04205
• DOI: 10.1002/humu.22467
• Languages: English
• ISSNs: 1059-7794