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Viable Neuronopathic Gaucher Disease Model in Medaka (Oryzias latipes) Displays Axonal Accumulation of Alpha-Synuclein
Homozygous mutations in the glucocerebrosidase (GBA) gene result in Gaucher disease (GD), the most common lysosomal storage disease. Recent genetic studies have revealed that GBA mutations confer a strong risk for sporadic Parkinson’s disease (PD). To investigate how GBA mutations cause PD, we gener...
Autores principales: | Uemura, Norihito, Koike, Masato, Ansai, Satoshi, Kinoshita, Masato, Ishikawa-Fujiwara, Tomoko, Matsui, Hideaki, Naruse, Kiyoshi, Sakamoto, Naoaki, Uchiyama, Yasuo, Todo, Takeshi, Takeda, Shunichi, Yamakado, Hodaka, Takahashi, Ryosuke |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Public Library of Science
2015
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4383526/ https://www.ncbi.nlm.nih.gov/pubmed/25835295 http://dx.doi.org/10.1371/journal.pgen.1005065 |
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