Spastic ataxia 4

MONDO:0013354

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, 0 tagged with Spastic ataxia 4 itself.

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↑ Mitochondrial oxidative phosphorylation disorder (58) ↑ Autosomal recessive spastic ataxia (1)

Including sub-types (14) Tagged with Spastic ataxia 4 (0)

We haven't found any trials for this condition yet. Follow it to get notified when new trials appear.