Modelling FUS Mislocalisation in an In Vitro Model of Innervated Human Muscle
Modelling FUS Mislocalisation in an In Vitro Model of Innervated Human Muscle
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New York: Springer US
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Language
English
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New York: Springer US
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Contents
Degeneration of distal axons and neuromuscular junctions is an early feature in the pathology of amyotrophic lateral sclerosis (ALS), which culminates in motor neuron loss due to axon retraction and muscle atrophy. The complex interactions in the pathogenesis of ALS between motor neurons, muscle cells and accompanying glia require an appropriate ex...
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Modelling FUS Mislocalisation in an In Vitro Model of Innervated Human Muscle
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TN_cdi_proquest_miscellaneous_1910800116
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https://devfeature-collection.sl.nsw.gov.au/record/TN_cdi_proquest_miscellaneous_1910800116
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ISSN
0895-8696
E-ISSN
1559-1166
DOI
10.1007/s12031-017-0940-y