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GBA1 mutations: Prospects for Exosomal Biomarkers in α-Synuclein Pathologies

The discovery that patients with Gaucher Disease (GD), a rare lysosomal storage disorder, were developing symptoms similar to Parkinson Disease (PD) led to investigation of the relationship between the two seemingly unrelated pathologies. GD, an autosomal recessive disorder, is the result of a biall...

पूर्ण विवरण

में बचाया:
ग्रंथसूची विवरण
में प्रकाशित:Mol Genet Metab
मुख्य लेखकों: Johnson, Parker, Weinreb, Neal J., Cloyd, James, Tuite, Paul J, Kartha, Reena V.
स्वरूप: Artigo
भाषा:Inglês
प्रकाशित: 2019
विषय:
ऑनलाइन पहुंच:https://ncbi.nlm.nih.gov/pmc/articles/PMC7002237/
https://ncbi.nlm.nih.gov/pubmed/31761523
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1016/j.ymgme.2019.10.006
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