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Autosomal dominant mutations in POLG and C10orf2: association with late onset chronic progressive external ophthalmoplegia and Parkinsonism in two patients

Brandon, Barton; Diederich, Nico; Soni, Madhu et al.

2013 • In Journal of Neurology, 260, p. 1931–1933

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Autosomal dominant mutations in POLG and C10orf2 association with late onset chronic progressive external ophthalmoplegia and Parkinsonism in two patients.pdf

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Autosomal dominant mutations in POLG and C10orf2 association with late onset chronic progressive external ophthalmoplegia and Parkinsonism in two patients.pdf

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