Ataxia - oculomotor apraxia type 4

Any oculomotor apraxia or related oculomotor disease in which the cause of the disease is a mutation in the PNKP gene.

Also known as: AOA4, PNKP oculomotor apraxia or related oculomotor disease, ataxia - oculomotor apraxia type 4, oculomotor apraxia or related oculomotor disease caused by mutation in PNKP, ataxia-oculomotor apraxia 4, ataxia-oculomotor apraxia-4

26 clinical trials for this condition and its sub-types.