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ENSpastic Ataxia 4
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Spastic Ataxia 4 is related to spastic ataxia 4, autosomal recessive and bile acid synthesis defect, congenital, 1, and has symptoms including paraparesis, spastic An important gene associated with Spastic Ataxia 4 is MTPAP (Mitochondrial Poly(A) Polymerase), and among its related pathways/superpathways is Translation factors. Related phenotype is Increased shRNA abundance (Z-score > 2).
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MALACARDS
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HPO Frequency
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MGI
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