Loss of the E3 ubiquitin ligase LRSAM1 sensitizes peripheral axons to degeneration in a mouse model of Charcot-Marie-Tooth disease

SUMMARY Charcot-Marie-Tooth disease (CMT) is a clinically and genetically heterogeneous condition characterized by peripheral axon degeneration with subsequent motor and sensory deficits. Several CMT gene products function in endosomal sorting and trafficking to the lysosome, suggesting that defects...

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Bibliographic Details
Main Authors: Laurent P. Bogdanik (Author), James N. Sleigh (Author), Cong Tian (Author), Mark E. Samuels (Author), Karen Bedard (Author), Kevin L. Seburn (Author), Robert W. Burgess (Author)
Format: Book
Published: The Company of Biologists, 2013-05-01T00:00:00Z.
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Call Number: A1234.567
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