Delayed Induction of Human NTE (PNPLA6) Rescues Neurodegeneration and Mobility Defects of Drosophila swiss cheese (sws) Mutants

Human PNPLA6 gene encodes Neuropathy Target Esterase protein (NTE). PNPLA6 gene mutations cause hereditary spastic paraplegia (SPG39 HSP), Gordon-Holmes syndrome, Boucher-Neuhäuser syndromes, Laurence-Moon syndrome, and Oliver-McFarlane syndrome. Mutations in the Drosophila NTE homolog swiss cheese...

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Detaylı Bibliyografya
Yayımlandı:PLoS One
Asıl Yazarlar: Sujkowski, Alyson, Rainier, Shirley, Fink, John K., Wessells, Robert J.
Materyal Türü: Artigo
Dil:Inglês
Baskı/Yayın Bilgisi: Public Library of Science 2015
Konular:
Research Article
Online Erişim:https://ncbi.nlm.nih.gov/pmc/articles/PMC4684404/
https://ncbi.nlm.nih.gov/pubmed/26671664
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1371/journal.pone.0145356
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