Amyotrophic Lateral Sclerosis · 2009 · 110 citations · 108 references
Life SciencesGeneticsMolecular GeneticsHuman GeneticsMedical GeneticsNeurogeneticsAmyotrophic Lateral SclerosisGenetic DisordersNeurodegenerative Disease GeneticsNeurodegenerative DiseasesNeurodegenerative DisordersNeurogenetic DisordersAssociation StudiesCopy Number ChangesCopy Number ControlFamilial Neurodegenerative DiseaseGenome-wide Association MappingHereditary Motor Neuron DiseaseNeurodegeneration GeneticsNeurodegenerative Genetics
The genetic causes of amyotrophic lateral sclerosis (ALS) are slowly being dissected out with the help of recent advances in genetic technology. Linkage studies and association studies examining candidate genes, candidate pathways, and genome-wide association have been used, based on direct sequencing and correlations between genetic variations. Copy number and microsatellite variants have also been examined, although the ideal methods for analysis are still being developed. In this review we examine the evidence for a genetic basis to ALS, discuss the challenges and difficulties faced and summarize the support for the reported genetic causes of ALS.
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Initial sequencing and analysis of the human genome
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TDP-43 Mutations in Familial and Sporadic Amyotrophic Lateral Sclerosis
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Life Sciences, Biology, Genetics +13