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- W2016010006 endingPage "273" @default.
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- W2016010006 abstract "Several genetic causes have been recently described for neurological diseases, increasing our knowledge of the common pathological mechanisms involved in these disorders. Mutation analysis has shown common causative factors for two major neurodegenerative disorders, ALS and FTD. Shared pathological and genetic markers as well as common neurological signs between these diseases have given rise to the notion of an ALS/FTD spectrum. This overlap among genetic factors causing ALS/FTD and the coincidence of mutated alleles (including causative, risk and modifier variants) have given rise to the notion of an oligogenic model of disease. In this review we summarize major advances in the elucidation of novel genetic factors in these diseases which have led to a better understanding of the common pathogenic factors leading to neurodegeneration." @default.
- W2016010006 created "2016-06-24" @default.
- W2016010006 creator A5002628021 @default.
- W2016010006 creator A5022091308 @default.
- W2016010006 creator A5031745517 @default.
- W2016010006 creator A5091192587 @default.
- W2016010006 date "2015-05-01" @default.
- W2016010006 modified "2023-10-17" @default.
- W2016010006 title "Defining the genetic connection linking amyotrophic lateral sclerosis (ALS) with frontotemporal dementia (FTD)" @default.
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