Phenotype of Amyotrophic Lateral Sclerosis (ALS) and Frontotemporal Dementia with ALS (FTD/ALS) Associated with the GGGGCC Repeat Expansion in C9ORF72 (c9FTD/ALS) (S05.003)
Explore this paper's citation graph
- Type
- article
- Published
- 2012-04-22
- Cited by
- 0
- References
- 0
- OpenAlex
- https://openalex.org/W4239639350
Keywords
C9orf72, Amyotrophic lateral sclerosis, Frontotemporal dementia, Medicine, TARDBP
References
No references recorded for this paper.
Cited by
No citing papers recorded for this paper.
Related papers
- Targeted Screening of the C9orf72 Gene in Bulgarian Amyotrophic Lateral Sclerosis Patients
- Pathogenic Genome Signatures That Damage Motor Neurons in Amyotrophic Lateral Sclerosis
- Emerging role of microRNAs in the pathogenesis of amyotrophic lateral sclerosis
- Frontotemporal dementia spectrum: first genetic screen in a Greek cohort
- Neuroimaging in genetic frontotemporal dementia and amyotrophic lateral sclerosis
- Genetic screening of a large series of North American sporadic and familial frontotemporal dementia cases
- Tale of two diseases: amyotrophic lateral sclerosis and frontotemporal dementia.
- C9orf72 hexanucleotide repeat expansions as the causative mutation for chromosome 9p21-linked amyotrophic lateral sclerosis and frontotemporal dementia.