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The C9ORF72 expansion mutation is a common cause of ALS+/−FTD in Europe and has a single founder
Download from www.nature.comClinico-pathological features in amyotrophic lateral sclerosis with expansions in C9ORF72
Download from doi.orgMolecular pathways of motor neuron injury in amyotrophic lateral sclerosis
Download from www.nature.comNovel FUS/TLS Mutations and Pathology in Familial and Sporadic Amyotrophic Lateral Sclerosis
Download from jamanetwork.comMutations in CHMP2B in lower motor neuron predominant amyotrophic lateral sclerosis (ALS)
Download from doi.orgHsp60 Is a Rare Cause of Hereditary Spastic Paraparesis, but May Act as a Genetic Modifier
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