Spastic ataxia 4

Any autosomal recessive spastic ataxia in which the cause of the disease is a mutation in the MTPAP gene.

Also known as: MTPAP autosomal recessive spastic ataxia, SPAX4, autosomal recessive spastic ataxia caused by mutation in MTPAP, autosomal recessive spastic ataxia type 4, spastic ataxia type 4, autosomal recessive spastic ataxia - optic atrophy - dysarthria, autosomal recessive spastic ataxia 4, autosomal recessive spastic ataxia-optic atrophy-dysarthria syndrome

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