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Case Reports
, 16 (8), 507-9

SANDO: Two Novel Mutations in POLG1 Gene

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Case Reports

SANDO: Two Novel Mutations in POLG1 Gene

Miguel Fernandes Gago et al. Neuromuscul Disord.

Abstract

Sensory ataxia with neuropathy, dysarthria and ophthalmoparesis represent the clinical triad of SANDO, a specific mitochondrial phenotype first reported in 1997 in association with multiple mitochondrial DNA deletions and mutations in POLG1 or more rarely in the C10orf2 (twinkle-helicase) gene. We report a 44-year-old man with SANDO who harboured two novel mutations (P648R/R807C) in the POLG1 gene.

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