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A neurodegenerative disease mutation that accelerates the clearance of apoptotic cells
Frontotemporal lobar degeneration is a progressive neurodegenerative syndrome that is the second most common cause of early-onset dementia. Mutations in the progranulin gene are a major cause of familial frontotemporal lobar degeneration [Baker M, et al. (2006) Nature 442:916–919 and Cruts M, et al....
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| Huvudupphovsmän: | , , , , , , , , , , , |
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| Materialtyp: | Artigo |
| Språk: | Inglês |
| Publicerad: |
National Academy of Sciences
2011
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| Ämnen: | |
| Länkar: | https://ncbi.nlm.nih.gov/pmc/articles/PMC3060230/ https://ncbi.nlm.nih.gov/pubmed/21368173 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1073/pnas.1100650108 |
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