PAW34 Mutations in OPA1 expand the clinical phenotype of mitochondrial disease | Journal of Neurology, Neurosurgery & Psychiatry

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PAW34 Mutations in OPA1 expand the clinical phenotype of mitochondrial disease

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Cite this article as:: Chinnery P, Jackson M, Amati-Bonneau P, et al

PAW34 Mutations in OPA1 expand the clinical phenotype of mitochondrial disease

Journal of Neurology, Neurosurgery & Psychiatry 2010;81:e32-e33.