O40 – 2159 Hypomyelinating leukodystrophy due to recessive mutations of GJC2 (connexin 47): clinical and radiological characteristics in 18 patients

✍ Scribed by Renaldo, F; Tonduti, D; Dorboz, I; Masliah, J; Giraud, G; Elmaleh, M; Orivoli, S; Beraud-Majorel, C; Drunat, S; Chalard, F; Barthez, MA; Desguerre, I; Quijano-Roy, S; Rodriguez, D; Boespflug-Tanguy, O

• Book ID: 122628466
• Publisher: Elsevier Science
• Year: 2013
• Tongue: English
• Weight: 70 KB
• Volume: 17
• Category: Article
• ISSN: 1090-3798
• DOI: 10.1016/S1090-3798(13)70042-4