| Issue |
Med Sci (Paris)
Volume 25, Number 3, Mars 2009
|
|
|---|---|---|
| Page(s) | 235 - 238 | |
| Section | Nouvelles | |
| DOI | https://doi.org/10.1051/medsci/2009253235 | |
| Published online | 15 March 2009 | |
Des mutations dans l’exon HSN2 du gène WNK1 causent la neuropathie héréditaire sensitive et autonomique de type 2
Mutations in the HSN2 exon of WNK1 cause hereditary sensory neuropathy type II
1
Centre d’excellence en neuromique de l’Université de Montréal (CENUM), 1560, rue Sherbrooke Est, Pavillon de-Sève, salle Y-3624, Montréal, Québec, H2L 4M1 Canada
2
Centre de Génétique, Hôpital d’Enfants, CHU Consultation de génétique, 10, boulevard Maréchal de Lattre de Tassigny, BP 77908, 21079 Dijon Cedex, France
3
Centre d’excellence en neuromique de l’Université de Montréal (CENUM), CHU Sainte-Justine, 3175 Côte-Ste-Catherine, salle A-733, Montréal, Québec, H3T 1C5 Canada
Cet article ne possède pas de résumé.
© 2009 médecine/sciences - Inserm / SRMS
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