VPS13C-Another Hint at Mitochondrial Dysfunction in Familial Parkinson's Disease

Affiliations

¹ Sobell Department of Motor Neuroscience and Movement Disorders, Institute of Neurology, London, UK.
² Department of Molecular Neuroscience, University College London Institute of Neurology, London, UK.

Comment

Sebastian R Schreglmann et al. Mov Disord. 2016 Sep.

. 2016 Sep;31(9):1340.

doi: 10.1002/mds.26682. Epub 2016 May 23.

¹ Sobell Department of Motor Neuroscience and Movement Disorders, Institute of Neurology, London, UK.
² Department of Molecular Neuroscience, University College London Institute of Neurology, London, UK.

No abstract available

Comment on

Loss of VPS13C Function in Autosomal-Recessive Parkinsonism Causes Mitochondrial Dysfunction and Increases PINK1/Parkin-Dependent Mitophagy.
Lesage S, Drouet V, Majounie E, Deramecourt V, Jacoupy M, Nicolas A, Cormier-Dequaire F, Hassoun SM, Pujol C, Ciura S, Erpapazoglou Z, Usenko T, Maurage CA, Sahbatou M, Liebau S, Ding J, Bilgic B, Emre M, Erginel-Unaltuna N, Guven G, Tison F, Tranchant C, Vidailhet M, Corvol JC, Krack P, Leutenegger AL, Nalls MA, Hernandez DG, Heutink P, Gibbs JR, Hardy J, Wood NW, Gasser T, Durr A, Deleuze JF, Tazir M, Destée A, Lohmann E, Kabashi E, Singleton A, Corti O, Brice A; French Parkinson's Disease Genetics Study (PDG); International Parkinson's Disease Genomics Consortium (IPDGC). Lesage S, et al. Am J Hum Genet. 2016 Mar 3;98(3):500-513. doi: 10.1016/j.ajhg.2016.01.014. Am J Hum Genet. 2016. PMID: 26942284 Free PMC article.