Phenotypical characteristics of idiopathic infantile nystagmus with and without mutations in FRMD7. [electronic resource]
Producer: 20080616Description: 1259-67 p. digitalISSN:- 1460-2156
- Adolescent
- Adult
- Aged
- Aged, 80 and over
- Child
- Child, Preschool
- Chromosomes, Human, X -- genetics
- Color Perception
- Cytoskeletal Proteins -- genetics
- Depth Perception
- Eye Diseases, Hereditary -- genetics
- Female
- Genetic Diseases, X-Linked -- genetics
- Head -- pathology
- Heterozygote
- Humans
- Male
- Membrane Proteins -- genetics
- Middle Aged
- Mutation
- Nystagmus, Congenital -- genetics
- Nystagmus, Pathologic -- genetics
- Pedigree
- Posture
- Strabismus -- genetics
- Visual Acuity
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Publication Type: Journal Article; Multicenter Study; Research Support, Non-U.S. Gov't
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