A Hexanucleotide Repeat Expansion in C9ORF72 Is the Cause of Chromosome 9p21-Linked ALS-FTD
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Open Access
- 21 September 2011
- journal article
- research article
- Published by Elsevier
- Vol. 72 (2) , 257-268
- https://doi.org/10.1016/j.neuron.2011.09.010
Abstract
No abstract availableKeywords
This publication has 35 references indexed in Scilit:
- Expanded GGGGCC Hexanucleotide Repeat in Noncoding Region of C9ORF72 Causes Chromosome 9p-Linked FTD and ALSPublished by Elsevier ,2011
- The chromosome 9 ALS and FTD locus is probably derived from a single founderNeurobiology of Aging, 2011
- Expansion of Intronic GGCCTG Hexanucleotide Repeat in NOP56 Causes SCA36, a Type of Spinocerebellar Ataxia Accompanied by Motor Neuron InvolvementAmerican Journal of Human Genetics, 2011
- Exome Sequencing Reveals VCP Mutations as a Cause of Familial ALSNeuron, 2010
- Chromosome 9p21 in sporadic amyotrophic lateral sclerosis in the UK and seven other countries: a genome-wide association studyThe Lancet Neurology, 2010
- Chromosome 9p21 in amyotrophic lateral sclerosis in Finland: a genome-wide association studyThe Lancet Neurology, 2010
- Common variants at 7p21 are associated with frontotemporal lobar degeneration with TDP-43 inclusionsNature Genetics, 2010
- PLINK: A Tool Set for Whole-Genome Association and Population-Based Linkage AnalysesAmerican Journal of Human Genetics, 2007
- Transport-Dependent Proteolysis of SREBPCell, 1999
- Mutations in Cu/Zn superoxide dismutase gene are associated with familial amyotrophic lateral sclerosisNature, 1993