Autosomal recessive ataxias due to POLG mutations SANDO (Q106303)

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Mutation in the POLG1 gene coding for polymerase gamma 1 can cause a variety of heterogenous mitochondrial diseases due to accumulation of deletions of mitochondrial DNA. Sensory ataxia neuropathy dysarthria and ophthalmoplegia (SANDO) is a disorder that can result from POLG1 mutation.
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    Autosomal recessive ataxias due to POLG mutations SANDO
    Mutation in the POLG1 gene coding for polymerase gamma 1 can cause a variety of heterogenous mitochondrial diseases due to accumulation of deletions of mitochondrial DNA. Sensory ataxia neuropathy dysarthria and ophthalmoplegia (SANDO) is a disorder that can result from POLG1 mutation.

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      CID11:ID_1147398404
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      dki-india-ID_1147398404
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      Concluído
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      16 August 2026
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