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  • Phenotypic and genetic exploration of severe demyelinating and secondary axonal neuropathies resulting from GDAP1 nonsense and splicing mutations

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Phenotypic and genetic exploration of severe demyelinating and secondary axonal neuropathies resulting from GDAP1 nonsense and splicing mutations

Authors

  1. Correspondence to:
 Dr N Lévy, Inserm U491, Génétique Médicale et Développement, Faculté de Médecine la Timone, 13385 Marseille Cedex 05, France; 
 nicolas.levy{at}medecine.univ-mrs.fr
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Citation

De Sandre-Giovannoli A, Chaouch M, Boccaccio I, et al
Phenotypic and genetic exploration of severe demyelinating and secondary axonal neuropathies resulting from GDAP1 nonsense and splicing mutations
Journal of Medical Genetics 2003;40:e87.

Publication history

  • First published July 1, 2003.
Online issue publication 
April 27, 2016

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Copyright 2003 Journal of Medical Genetics