Vanishing white matter disease with different faces

被引：0
|
作者：
Gülay Güngör
Olcay Güngör
Seda Çakmaklı
Hülya Maraş Genç
Hülya İnce
Gözde Yeşil
Cengiz Dilber
Kürşad Aydın
机构：
[1] Pamukkale University,Department of Radiology, Faculty of Medicine
[2] Pamukkale University,Department of Pediatric Neurology, Faculty of Medicine
[3] Necip Fazıl City Hospital,Department of Medical Genetics
[4] Ümraniye Training and Research Hospital,Department of Pediatric Neurology
[5] Medical Park University,Department of Pediatric Neurology, Faculty of Medicine
[6] Bezmialem Vakıf University,Department of Medical Genetics, Faculty of Medicine
[7] Medipol University,Department of Pediatric Neurology, Faculty of Medicine
[8] Marash Life Hospital,Department of Pediatric Neurology
来源：
Child's Nervous System | 2020年 / 36卷
关键词：
Brugada syndrome; EIF2B gene; Epilepsy; MRI; Vanishing white matter (VWM);
D O I：
暂无
中图分类号：
学科分类号：
摘要：
引用
收藏
页码：353 / 361
页数：8
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