Ataxia with oculomotor apraxia type 2 (AOA2): an eye movement study of two siblings

MeSH terms

• Apraxias* / complications
• Apraxias* / diagnostic imaging
• Apraxias* / genetics
• Cogan Syndrome* / complications
• Cogan Syndrome* / diagnostic imaging
• Cogan Syndrome* / genetics
• Eye Movements
• Humans
• Mutation
• Siblings
• Spinocerebellar Ataxias* / complications
• Spinocerebellar Ataxias* / congenital
• Spinocerebellar Ataxias* / diagnostic imaging
• Spinocerebellar Ataxias* / genetics