P601T mutation in Nav 1.7 sodium channel in a family with primary erythermalgia

Justine Avez-Couturier; Serge  Dalmas; Anouck Deprez; Louis Vallée

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Avez-Couturier J, Dalmas S, Deprez A and Vallée L P601T mutation in Nav 1.7 sodium channel in a family with primary erythermalgia. F1000Posters 2013, 4:1255 (poster)

P601T mutation in Nav 1.7 sodium channel in a family with primary erythermalgia

Justine Avez-Couturier¹, Justine Avez-Couturier², Justine Avez-Couturier³, Serge Dalmas, Anouck Deprez, Louis Vallée

Published 06 Nov 2013

Author Affiliations

¹ Service de Neurologie Pédiatrique, Hôpital Roger Salengro, CHRU de Lille, France
² Laboratoire INSERM CIC-IT 807 "Biocapteurs et eSanté ", CHRU de Lille, France
³ Consultation Douleur Enfant, CHRU de Lille, France

Copyright © 2013 Avez-Couturier J et al. This is an open access work distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.

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Published 06 Nov 2013

P601T mutation in Nav 1.7 sodium channel in a family with primary erythermalgia [version 1; not peer reviewed]

Justine Avez-Couturier¹, Justine Avez-Couturier², Justine Avez-Couturier³, Serge Dalmas, Anouck Deprez, Louis Vallée

Author Affiliations

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8th EFIC Congress “Pain in Europe” 2013

Abstract

Competing Interests

No competing interests were disclosed

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