Genetic and functional characterisation of ALS-linked genes TBK1, OPTN and MATR3

Amyotrophic Lateral Sclerosis (ALS) is a degenerative disease predominantly affecting motor neurons in the brain and spinal cord. ALS has a clear genetic component, with mutations in four genes accounting for ~50% of familial and ~10% of sporadic cases. Several other rarer ALS genes have been identi...

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Bibliographic Details
Main Author: De Majo, Martina
Other Authors: Smith, Bradley Neville ; Shaw, Christopher Edward Dennistoun
Published: King's College London (University of London) 2018
Online Access:https://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.745410