טוען...
Neurodegenerative phenotypes in an A53T α-synuclein transgenic mouse model are independent of LRRK2
Mutations in the genes encoding LRRK2 and α-synuclein cause autosomal dominant forms of familial Parkinson's disease (PD). Fibrillar forms of α-synuclein are a major component of Lewy bodies, the intracytoplasmic proteinaceous inclusions that are a pathological hallmark of idiopathic and certai...
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| Main Authors: | , , , , , , , , , , |
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| פורמט: | Artigo |
| שפה: | Inglês |
| יצא לאור: |
Oxford University Press
2012
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| נושאים: | |
| גישה מקוונת: | https://ncbi.nlm.nih.gov/pmc/articles/PMC3349422/ https://ncbi.nlm.nih.gov/pubmed/22357653 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1093/hmg/dds057 |
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