Mutations in heat shock protein beta-1 (HSPB1) are associated with a range of clinical phenotypes related to different patterns of motor neuron dysfunction: A case series
Author:
Publisher
Elsevier BV
Subject
Clinical Neurology,Neurology
Reference51 articles.
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2. Hsp27 upregulation and phosphorylation is required for injured sensory and motor neuron survival;Benn;Neuron.,2002
3. HSPB1 mutations causing hereditary neuropathy in humans disrupt non-cell autonomous protection of motor neurons;Heilman;Exp. Neurol.,2017
4. A mutation in the small heat-shock protein HSPB1 leading to distal hereditary motor neuronopathy disrupts neurofilament assembly and the axonal transport of specific cellular cargoes;Ackerley;Hum. Mol. Genet.,2006
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