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Autosomal recessive ataxia due to PEX10 deficiency

MONDO:0016614

Also known as: mild peroxismal disorder due to PEX10 deficiency

18 clinical trials for this condition and its sub-types, 0 tagged with Autosomal recessive ataxia due to PEX10 deficiency itself.

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