Zobrazeno 1 - 2
of 2
pro vyhledávání: '"Mathew J. Rybin"'
Autor:
Nadja S. Andrade, Melina Ramic, Rustam Esanov, Wenjun Liu, Mathew J. Rybin, Gabriel Gaidosh, Abbas Abdallah, Samuel Del’Olio, Tyler C. Huff, Nancy T. Chee, Sadhana Anatha, Tania F. Gendron, Claes Wahlestedt, Yanbin Zhang, Michael Benatar, Christian Mueller, Zane Zeier
Publikováno v:
Molecular Neurodegeneration, Vol 15, Iss 1, Pp 1-18 (2020)
Abstract Background The C9ORF72 hexanucleotide repeat expansion is the most common known genetic cause of amyotrophic lateral sclerosis (ALS) and frontotemporal dementia (FTD), two fatal age-related neurodegenerative diseases. The C9ORF72 expansion e
Externí odkaz:
https://doaj.org/article/5b25cbfded474c1cbe5d4990bc503838
Autor:
Christian Mueller, Melina Ramic, Abbas Abdallah, Tania F. Gendron, Zane Zeier, Rustam Esanov, Mathew J. Rybin, Sadhana Anatha, Michael Benatar, Tyler C. Huff, Gabriel Gaidosh, Samuel Del’Olio, Claes Wahlestedt, Nancy T. Chee, Nadja S. Andrade, Wenjun Liu, Yanbin Zhang
Publikováno v:
Molecular Neurodegeneration, Vol 15, Iss 1, Pp 1-18 (2020)
Molecular Neurodegeneration
Molecular Neurodegeneration
Background The C9ORF72 hexanucleotide repeat expansion is the most common known genetic cause of amyotrophic lateral sclerosis (ALS) and frontotemporal dementia (FTD), two fatal age-related neurodegenerative diseases. The C9ORF72 expansion encodes fi
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::f354bf00808ba6a343650fae5d17955b
https://doi.org/10.1186/s13024-020-00365-9
https://doi.org/10.1186/s13024-020-00365-9