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Primary Coenzyme Q10 Deficiency 9
A coenzyme Q10 deficiency disease characterized by onset in the first decade of life of cerebellar ataxia associated with cerebellar atrophy that is caused by mutation homozygous or compound heterozygous in the COQ5 gene
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When to seek help
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Overview
A coenzyme Q10 deficiency disease characterized by onset in the first decade of life of cerebellar ataxia associated with cerebellar atrophy that is caused by mutation homozygous or compound heterozygous in the COQ5 gene
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