Media type: E-Article Title: Chilren with ocular motor apraxia type Cogan carry deletions in the gene (NPHP1) for juvenile nephronopthisis Contributor: Betz, Regina; Rensing, Cornelia; Otto, Edgar; Mincheva, Antoaneta; Zebnder, Daniel; Lichter, Peter; Hildebrandt, Friedhelm imprint: Elsevier BV, 2000 Published in: The Journal of Pediatrics Language: English DOI: 10.1016/s0022-3476(00)01001-5 ISSN: 0022-3476 Keywords: Pediatrics, Perinatology and Child Health Origination: Footnote: