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Des mutations dans l’exon HSN2 du gène WNK1 causent la neuropathie héréditaire sensitive et autonomique de type 2

Jean-Baptiste Rivière, Patrick Dion, Masoud Shekarabi, Nathalie Girard, Laurence Faivre, Ronald G. Lafrenière, Mark Samuels and Guy A. Rouleau

Med Sci (Paris), 25 3 (2009) 235-238

Published online: 15 March 2009

DOI: 10.1051/medsci/2009253235

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médecine/sciences

Chief editor: Anna Salvetti - Deputy-chief editors: Hélène Dutartre, Henri Gruffat
Chief copy editor: François Flori - Associate editor: Jean-Pierre Hardelin - Editorial board
ISSN: 0767-0974 - eISSN: 1958-5381
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