The genetic architecture of amyotrophic lateral sclerosis (ALS) is being increasingly understood. In this far-reaching review, we examine what is currently known about ALS genetics and how these genes were initially identified. We also discuss the various types of mutations that might underlie this fatal neurodegenerative condition and outline some of the strategies that might be useful in untangling them. These include expansions of short repeat sequences, common and low-frequency genetic variations, de novo mutations, epigenetic changes, somatic mutations, epistasis, oligogenic and polygenic hypotheses.

Marangi, G., Traynor, B., Genetic causes of amyotrophic lateral sclerosis: new genetic analysis methodologies entailing new opportunities and challenges, <<BRAIN RESEARCH>>, N/A; (N/A): N/A-N/A. [doi:10.1016/j.brainres.2014.10.009] [http://hdl.handle.net/10807/61171]

Genetic causes of amyotrophic lateral sclerosis: new genetic analysis methodologies entailing new opportunities and challenges

Marangi, Giuseppe;
2014

Abstract

The genetic architecture of amyotrophic lateral sclerosis (ALS) is being increasingly understood. In this far-reaching review, we examine what is currently known about ALS genetics and how these genes were initially identified. We also discuss the various types of mutations that might underlie this fatal neurodegenerative condition and outline some of the strategies that might be useful in untangling them. These include expansions of short repeat sequences, common and low-frequency genetic variations, de novo mutations, epigenetic changes, somatic mutations, epistasis, oligogenic and polygenic hypotheses.
2014
Inglese
Marangi, G., Traynor, B., Genetic causes of amyotrophic lateral sclerosis: new genetic analysis methodologies entailing new opportunities and challenges, <<BRAIN RESEARCH>>, N/A; (N/A): N/A-N/A. [doi:10.1016/j.brainres.2014.10.009] [http://hdl.handle.net/10807/61171]
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Utilizza questo identificativo per citare o creare un link a questo documento: https://hdl.handle.net/10807/61171
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