Mutations in FRMD7, a newly identified member of the FERM family, cause X-linked idiopathic congenital nystagmus
- 1 October 2006
- journal article
- research article
- Published by Springer Nature in Nature Genetics
- Vol. 38 (11) , 1242-1244
- https://doi.org/10.1038/ng1893
Abstract
No abstract availableKeywords
This publication has 15 references indexed in Scilit:
- FARP2 triggers signals for Sema3A-mediated axonal repulsionNature Neuroscience, 2005
- Social and visual function in nystagmusBritish Journal of Ophthalmology, 2005
- Coot: model-building tools for molecular graphicsActa Crystallographica Section D-Biological Crystallography, 2004
- Confirmation and refinement of a genetic locus of congenital motor nystagmus in Xq26.3-q27.1 in a Chinese familyHuman Genetics, 2004
- Distinguishing stimulus-driven behavior from random responding in psychophysical tests of infants' optic flow discriminationJournal of Vision, 2004
- Congenital nystagmus: Hypotheses for its genesis and complex waveforms within a behavioral ocular motor system modelJournal of Vision, 2004
- Announcing the worldwide Protein Data BankNature Structural & Molecular Biology, 2003
- NystagmusCurrent Opinion in Opthalmology, 2001
- Congenital Motor Nystagmus Linked to Xq26-q27American Journal of Human Genetics, 1999
- Ocular and vision defects in preschool children.British Journal of Ophthalmology, 1993