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Investigating FUS variation in Parkinson’s disease
Mutations of the FUS gene were first reported to cause amyotrophic lateral sclerosis (ALS). Subsequent studies confirmed the role of mutations in ALS and also implicated them in frontotemporal dementia (FTD). Recently, through Next-Generation Exome sequencing approaches a mutation resulting in a sub...
Tallennettuna:
| Julkaisussa: | Parkinsonism Relat Disord |
|---|---|
| Päätekijät: | , , , , , , |
| Aineistotyyppi: | Artigo |
| Kieli: | Inglês |
| Julkaistu: |
2014
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| Aiheet: | |
| Linkit: | https://ncbi.nlm.nih.gov/pmc/articles/PMC4721223/ https://ncbi.nlm.nih.gov/pubmed/24262168 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1016/S1353-8020(13)70035-X |
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