Clogging information flow in ALS

dc.contributor.authorJoseph W. Paul IIIen_US
dc.contributor.authorAaron D. Gitleren_US
dc.date.accessioned2014-11-17T13:39:26Z
dc.date.available2014-11-17T13:39:26Z
dc.date.issued2014-09-05
dc.description.abstractAmyotrophic lateral sclerosis (ALS), also known as Lou Gehrig's disease, is a devastating neurodegenerative disorder that causes a progressive loss of motor neurons, leading to paralysis and death typically within 2 to 5 years of onset. There are no cures and few treatments. ALS shares some genetic and pathological overlap with another neurodegenerative disease, frontotemporal dementia (FTD), which causes changes to personality and language. Mutations in the gene called chromosome 9 open reading frame 72 (C9orf72) are the most common genetic cause of both ALS and FTD. This is the author’s version of the work. It is posted here by permission of the AAAS for personal use, not for redistribution. The definitive version was published in Science on [Volume 345 on 5 September 2014], DOI: 10.1126/science.1259461.en_US
dc.identifier.citationScience; 345:6201 p. 1118-1119en_US
dc.identifier.doi10.1126/science.1259461
dc.identifier.pmid25190778en_US
dc.identifier.urihttp://hdl.handle.net/10342/4589
dc.language.isoen_USen_US
dc.relation.urihttp://www.sciencemag.org/content/345/6201/1118.summaryen_US
dc.subjectAmyotrophic lateral sclerosisen_US
dc.subjectNeurodegenerationen_US
dc.subjectALSen_US
dc.subjectFrontotemporal dementiaen_US
dc.subjectFTDen_US
dc.subjectNucleolusen_US
dc.subjectHuman geneticsen_US
dc.subjectProteotoxicityen_US
dc.titleClogging information flow in ALSen_US
dc.title.alternativeCell Biology. Clogging information flow in ALS.en_US
dc.typeArticleen_US
ecu.journal.issue6201
ecu.journal.nameScience
ecu.journal.pages1118-1119
ecu.journal.volume345

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