Distinct neurological disorders with C9orf72 mutations: genetics, pathogenesis, and therapy
Author:
Publisher
Elsevier BV
Subject
Behavioral Neuroscience,Cognitive Neuroscience,Neuropsychology and Physiological Psychology
Reference141 articles.
1. A blinded international study on the reliability of genetic testing for GGGGCC-repeat expansions in C9orf72 reveals marked differences in results among 14 laboratories;Akimoto;J. Med. Genet.,2014
2. Repeat expansion in C9orf72 is not a major cause of amyotrophic lateral sclerosis among Iranian patients;Alavi;Neurobiol. Aging,2014
3. Early onset behavioral variant frontotemporal dementia due to the C9orf72 hexanucleotide repeat expansion: psychiatric clinical presentations;Arighi;J. Alzheimers Dis.,2012
4. Accumulation of dipeptide repeat proteins predates that of TDP-43 in Frontotemporal Lobar Degeneration associated with hexanucleotide repeat expansions in C9orf72 gene;Baborie;Neuropathol. Appl. Neurobiol.,2014
5. Large C9orf72 hexanucleotide repeat expansions are seen in multiple neurodegenerative syndromes and are more frequent than expected in the UK population;Beck;Am. J. Hum. Genet.,2013
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