Novel Mutations in TARDBP (TDP-43) in Patients with Familial Amyotrophic Lateral Sclerosis

The TAR DNA-binding protein 43 (TDP-43) has been identified as the major disease protein in amyotrophic lateral sclerosis (ALS) and frontotemporal lobar degeneration with ubiquitin inclusions (FTLD-U), defining a novel class of neurodegenerative conditions: the TDP-43 proteinopathies. The first path...

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Detalhes bibliográficos
Main Authors: Rutherford, Nicola J., Zhang, Yong-Jie, Baker, Matt, Gass, Jennifer M., Finch, NiCole A., Xu, Ya-Fei, Stewart, Heather, Kelley, Brendan J., Kuntz, Karen, Crook, Richard J. P., Sreedharan, Jemeen, Vance, Caroline, Sorenson, Eric, Lippa, Carol, Bigio, Eileen H., Geschwind, Daniel H., Knopman, David S., Mitsumoto, Hiroshi, Petersen, Ronald C., Cashman, Neil R., Hutton, Mike, Shaw, Christopher E., Boylan, Kevin B., Boeve, Bradley, Graff-Radford, Neill R., Wszolek, Zbigniew K., Caselli, Richard J., Dickson, Dennis W., Mackenzie, Ian R., Petrucelli, Leonard, Rademakers, Rosa
Formato: Artigo
Idioma:Inglês
Publicado em: Public Library of Science 2008
Assuntos:
Research Article
Acesso em linha:https://ncbi.nlm.nih.gov/pmc/articles/PMC2527686/
https://ncbi.nlm.nih.gov/pubmed/18802454
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1371/journal.pgen.1000193
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