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Sensory and motor neuronopathy in a patient with the A382P TDP-43 mutation

Camdessanché, Jean-Philippe ; Belzil, Véronique V ; Jousserand, Guillemette ; Rouleau, Guy A ; Créac'H, Christelle ; Convers, Philippe ; Antoine, Jean-Christophe

Orphanet Journal of Rare Diseases, 2011, Vol.6, p.4-4 [Peer Reviewed Journal]

U.S. National Library of Medicine (NIH/NLM)

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Sensory and motor neuronopathy in a patient with the A382P TDP-43 mutation

Camdessanché, Jean-Philippe ; Belzil, Véronique V ; Jousserand, Guillemette ; Rouleau, Guy A ; Créac'H, Christelle ; Convers, Philippe ; Antoine, Jean-Christophe

Orphanet journal of rare diseases, 05 February 2011, Vol.6, pp.4 [Peer Reviewed Journal]

MEDLINE/PubMed (U.S. National Library of Medicine)

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Sensory and motor neuronopathy in a patient with the A382P TDP-43 mutation

Camdessanché, Jean-Philippe ; Belzil, Véronique ; Jousserand, Guillemette ; Rouleau, Guy ; Créac'H, Christelle ; Convers, Philippe ; Antoine, Jean-Christophe

Orphanet Journal of Rare Diseases, 2011, p.4 [Peer Reviewed Journal]

© ProQuest LLC All rights reserved

Full text available

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Material Type:
Article
Add to e-Shelf

Sensory and motor neuronopathy in a patient with the A382P TDP-43 mutation.

Camdessanché, Jean-Philippe ; Belzil, Véronique V ; Jousserand, Guillemette ; Rouleau, Guy A ; Créac'H, Christelle ; Convers, Philippe ; Antoine, Jean-Christophe Camdessanché, Jean-Philippe (correspondence author) ; Camdessanché, Jean-Philippe (record owner)

Orphanet journal of rare diseases, February 5, 2011, Vol.6, p.4 [Peer Reviewed Journal]

© ProQuest LLC All rights reserved

Full text available

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