Analysis of theC9orf72Gene in Patients with Amyotrophic Lateral Sclerosis in Spain and Different Populations Worldwide
出版年份 2012 全文链接
标题
Analysis of theC9orf72Gene in Patients with Amyotrophic Lateral Sclerosis in Spain and Different Populations Worldwide
作者
关键词
-
出版物
HUMAN MUTATION
Volume 34, Issue 1, Pages 79-82
出版商
Wiley
发表日期
2012-08-31
DOI
10.1002/humu.22211
参考文献
相关参考文献
注意：仅列出部分参考文献，下载原文获取全部文献信息。- Clinical characteristics of patients with familial amyotrophic lateral sclerosis carrying the pathogenic GGGGCC hexanucleotide repeat expansion of C9ORF72
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- Phenotype difference between ALS patients with expanded repeats inC9ORF72and patients with mutations in other ALS-related genes
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- Cognitive and clinical characteristics of patients with amyotrophic lateral sclerosis carrying a C9orf72 repeat expansion: a population-based cohort study
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- High frequency of the expanded C9ORF72 hexanucleotide repeat in familial and sporadic Greek ALS patients
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- Amyotrophic lateral sclerosis
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- A C9orf72 promoter repeat expansion in a Flanders-Belgian cohort with disorders of the frontotemporal lobar degeneration-amyotrophic lateral sclerosis spectrum: a gene identification study
- (2011) Ilse Gijselinck et al. LANCET NEUROLOGY
- The chromosome 9 ALS and FTD locus is probably derived from a single founder
- (2011) Kin Mok et al. NEUROBIOLOGY OF AGING
- Expanded GGGGCC Hexanucleotide Repeat in Noncoding Region of C9ORF72 Causes Chromosome 9p-Linked FTD and ALS
- (2011) Mariely DeJesus-Hernandez et al. NEURON
- A Hexanucleotide Repeat Expansion in C9ORF72 Is the Cause of Chromosome 9p21-Linked ALS-FTD
- (2011) Alan E. Renton et al. NEURON
- Dementia and cognitive impairment in amyotrophic lateral sclerosis: a review
- (2010) Maria Teresa Giordana et al. NEUROLOGICAL SCIENCES
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