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PrintAny oculomotor apraxia or related oculomotor disease in which the cause of the disease is a mutation in the PNKP gene.
MedlinePlus has information about this condition that may include a description, frequency, causes, inheritance, and links to more information. The information is written for the public, including patients, caregivers and families. MedlinePlus is a service of the National Library of Medicine (NLM), which is part of the National Institutes of Health (NIH).
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