POLG1 mutations cause a syndromic epilepsy with occipital lobe predilection.
Bernt A. Engelsen; Charalampos Tzoulis; Bjørn Karlsen; Atle Lillebø; Liv M. Lægreid; Jan Aasly; Massimo Zeviani; Laurence A. Bindoff; Brain: A Journal of Neurology, 2008, vol. 131, issue 3, p 818, ISSN 00068950. ISBN 14602156.

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