Publication Date
| In 2026 | 0 |
| Since 2025 | 0 |
| Since 2022 (last 5 years) | 0 |
| Since 2017 (last 10 years) | 0 |
| Since 2007 (last 20 years) | 1 |
Descriptor
| Comparative Analysis | 1 |
| Depth Perception | 1 |
| Eye Movements | 1 |
| Genetics | 1 |
| Human Body | 1 |
| Infants | 1 |
| Patients | 1 |
| Visual Acuity | 1 |
| Visual Impairments | 1 |
Source
| Brain | 1 |
Author
| Awan, Musarat | 1 |
| Degg, Chris | 1 |
| Farooq, Shegufta J. | 1 |
| Gale, Richard P. | 1 |
| Gottlob, Irene | 1 |
| Jain, Sunila | 1 |
| Kumar, A. S. Anil | 1 |
| Langmann, Andrea | 1 |
| Lindner, Susanne | 1 |
| McLean, Rebecca | 1 |
| Proudlock, Frank A. | 1 |
| More ▼ | |
Publication Type
| Journal Articles | 1 |
| Reports - Research | 1 |
Education Level
Audience
Location
Laws, Policies, & Programs
Assessments and Surveys
What Works Clearinghouse Rating
Phenotypical Characteristics of Idiopathic Infantile Nystagmus with and without Mutations in "FRMD7"
Peer reviewed
Direct linkThomas, Shery; Proudlock, Frank A.; Sarvananthan, Nagini; Roberts, Eryl O.; Awan, Musarat; McLean, Rebecca; Surendran, Mylvaganam; Kumar, A. S. Anil; Farooq, Shegufta J.; Degg, Chris; Gale, Richard P.; Reinecke, Robert D.; Woodruff, Geoffrey; Langmann, Andrea; Lindner, Susanne; Jain, Sunila; Tarpey, Patrick; Raymond, F. Lucy; Gottlob, Irene – Brain, 2008
Idiopathic infantile nystagmus (IIN) consists of involuntary oscillations of the eyes. The familial form is most commonly X-linked. We recently found mutations in a novel gene "FRMD7" (Xq26.2), which provided an opportunity to investigate a genetically defined and homogeneous group of patients with nystagmus. We compared clinical features and eye…
Descriptors: Visual Impairments, Eye Movements, Visual Acuity, Depth Perception
