1. SCN10A variants associated with congenital harlequin syndrome. (1st June 2022) Authors: Halle, Aurelie; De Becdelievre, Alix; Funalot, Benoit; Labrèze, Christine; Morice‐Picard, Fanny; Boralevi, Franck Journal: British journal of dermatology Issue: Volume 186:Number 6(2022) Page Start: 1039 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
2. SCN10A variants associated with congenital harlequin syndrome. (22nd March 2022) Authors: Halle, Aurelie; De Becdelievre, Alix; Funalot, Benoit; Labrèze, Christine; Morice‐Picard, Fanny; Boralevi, Franck Journal: British journal of dermatology Issue: Volume 186:Number 6(2022) Page Start: 1039 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗