Sensory neuronopathy in patients harbouring recessive polymerase γ mutations

POLG, but notPEO1, is a frequent cause of cerebellar ataxia in Central Europe

(2010) Julia Schicks et al.   MOVEMENT DISORDERS

Sensory ataxic neuropathy with dysarthria and ophthalmoparesis (SANDO) in late life due to compound heterozygous POLG mutations

(2010) Michael D. Weiss et al.   MUSCLE & NERVE

Rare Autosomal Dominant POLG1 Mutation in a Family With Metabolic Strokes, Posterior Column Spinal Degeneration, and Multi-Endocrine Disease

(2009) Sarah E. Hopkins et al.   JOURNAL OF CHILD NEUROLOGY

Novel POLG1 mutations associated with neuromuscular and liver phenotypes in adults and children

(2009) J D Stewart et al.   JOURNAL OF MEDICAL GENETICS

A variable neurodegenerative phenotype with polymerase   mutation

(2009) S Stricker et al.   JOURNAL OF NEUROLOGY NEUROSURGERY AND PSYCHIATRY

ATAXIA WITH OPHTHALMOPLEGIA OR SENSORY NEUROPATHY IS FREQUENTLY CAUSED BY POLG MUTATIONS

(2009) C. Schulte et al.   NEUROLOGY