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of 2
pro vyhledávání: '"Ali Al Abdulatif"'
Autor:
Peter E. A. Ash, Elizabeth A. Stanford, Ali Al Abdulatif, Alejandra Ramirez-Cardenas, Heather I. Ballance, Samantha Boudeau, Amanda Jeh, James M. Murithi, Yorghos Tripodis, George J. Murphy, David H. Sherr, Benjamin Wolozin
Publikováno v:
Molecular Neurodegeneration, Vol 12, Iss 1, Pp 1-14 (2017)
Abstract Background Amyotrophic lateral sclerosis (ALS) is a debilitating neurodegenerative condition that is characterized by progressive loss of motor neurons and the accumulation of aggregated TAR DNA Binding Protein-43 (TDP-43, gene: TARDBP). Inc
Externí odkaz:
https://doaj.org/article/918a0164aa8e4ba8b9e5f89dd64cfaf5
Autor:
Yorghos Tripodis, Alejandra Ramirez-Cardenas, David H. Sherr, George J. Murphy, Heather I. Ballance, James M. Murithi, Peter E.A. Ash, Samantha Boudeau, Ali Al Abdulatif, Benjamin Wolozin, Elizabeth A. Stanford, Amanda Jeh
Publikováno v:
Molecular Neurodegeneration, Vol 12, Iss 1, Pp 1-14 (2017)
Molecular Neurodegeneration
Molecular Neurodegeneration
Background Amyotrophic lateral sclerosis (ALS) is a debilitating neurodegenerative condition that is characterized by progressive loss of motor neurons and the accumulation of aggregated TAR DNA Binding Protein-43 (TDP-43, gene: TARDBP). Increasing e
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::c78fb1b562920d58e0838ec8fe203ced
http://link.springer.com/article/10.1186/s13024-017-0177-9
http://link.springer.com/article/10.1186/s13024-017-0177-9