Congenital Ocular Motor Apraxia
References
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- Betz R Rensing C Otto E Mincheva A Zehnder D Lichter P Children with ocular motor apraxia type Cogan carry deletions in the gene (NPHP1) for juvenile nephronophthisis J Pediatr 2000 Jun 136 6 828 31 10.1067/mpd.2000.106225 10839884
DOI: https://doi.org/10.15844/pedneurbriefs-21-6-5 | Journal eISSN: 2166-6482
Language: English
Page range: 45 - 46
Published on: Jun 1, 2007
Published by: Pediatric Neurology Briefs Publishers
In partnership with: Paradigm Publishing Services
© 2007 J Gordon Millichap, published by Pediatric Neurology Briefs Publishers
This work is licensed under the Creative Commons Attribution 4.0 License.