Electromyographical and Motor Performance Studies in thepmnMouse Model of Neurodegenerative Disease

The mouse autosomal recessive mutation progressive motor neuronopathy (pmn) results in early onset motor neuron disease with rapidly progressive hindlimb paralysis, severe muscular wasting, and death at around 6 weeks of age. This mutant provides opportunities for testing novel therapeutic strategie...

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Bibliographic Details
Main Authors: Philippe F. Kennel, Paul Fonteneau, Elisabeth Martin, Jean-Marc Schmidt, Mimoun Azzouz, Jacques Borg, Jean-Louis Guenet, Henning Schmalbruch, Jean-Marie Warter, Philippe Poindron
Format: Article
Language:English
Published: Elsevier 1996-04-01
Series:Neurobiology of Disease
Online Access:http://www.sciencedirect.com/science/article/pii/S0969996196900145