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Author/Creator Roubergue, Anne

1. Novel KCNQ2 and KCNQ3 Mutations in a Large Cohort of Families with Benign Neonatal Epilepsy: First Evidence for an Altered Channel Regulation by Syntaxin‐1A. Issue 3 (13th January 2014)

Authors:
Soldovieri, Maria Virginia; Boutry‐Kryza, Nadia; Milh, Mathieu; Doummar, Diane; Heron, Benedicte; Bourel, Emilie; Ambrosino, Paolo; Miceli, Francesco; De, Michela; Dorison, Nathalie; Auvin, Stephane; Echenne, Bernard; Oertel, Julie; Riquet, Audrey; Lambert, Laetitia; Gerard, Marion; Roubergue, An...
Journal:
Human mutation
Issue:
Volume 35:Issue 3(2014:Mar.)
Page Start:
356
Record Type:
Journal Article
View Content:
Available online (eLD content is only available in our Reading Rooms) ↗

2. The multiple faces of the ATP1A3‐related dystonic movement disorder. Issue 10 (8th March 2013)

Authors:
Roubergue, Anne; Roze, Emmanuel; Vuillaumier‐Barrot, Sandrine; Fontenille, Marie‐Joséphine; Méneret, Aurélie; Vidailhet, Marie; Fontaine, Bertrand; Doummar, Diane; Philibert, Bertrand; Riant, Florence; Nicole, Sophie
Journal:
Movement disorders
Issue:
Volume 28:Issue 10(2013)
Page Start:
1457
Record Type:
Journal Article
View Content:
Available online (eLD content is only available in our Reading Rooms) ↗

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