Single heterozygous mutations in atp13a2 cause mitochondrial dysfunction

Jin Sung Park; Christine Klein; Carolyn M Sue

doi:10.1136/jnnp-2017-316074.69

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Abstracts

Single heterozygous mutations in atp13a2 cause mitochondrial dysfunction

Authors

Jin Sung Park Royal North Shore Hospital, Sydney, NSW, AustraliaDepartment of Neurogenetics, Kolling Institute, University of Sydney, St. Leonards PubMed articles Google scholar articles
Christine Klein Institute of Neurogenetics, University of Lübeck, Lübeck, Germany PubMed articles Google scholar articles
Carolyn M Sue Royal North Shore Hospital, Sydney, NSW, AustraliaDepartment of Neurogenetics, Kolling Institute, University of Sydney, St. Leonards PubMed articles Google scholar articles

Citation

Park JS, Klein C, Sue CM

Single heterozygous mutations in atp13a2 cause mitochondrial dysfunction

Journal of Neurology, Neurosurgery & Psychiatry 2017;88:e1.

Publication history

First published May 8, 2017.

Online issue publication

May 08, 2017

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