Genetic and neurodevelopmental spectrum of SYNGAP1-associated intellectual disability and epilepsy (vol 53, pg 511, 2016)

被引：5
|
作者：
Mignot, C.
von Stulpnagel, C.
Nava, C.
Ville, D.
Sanlaville, D.
Lesca, G.
Rastetter, A.
Gachet, B.
Marie, Y.
Korenke, G. C.
Borggraefe, I
Hoffmann-Zacharska, D.
Szczepanik, E.
Rudzka-Dybala, M.
Yis, U.
Caglayan, H.
Isapof, A.
Marey, I
Panagiotakaki, E.
Korff, C.
Rossier, E.
Riess, A.
Beck-Woedl, S.
Rauch, A.
Zweier, C.
Hoyer, J.
Reis, A.
Mironov, M.
Bobylova, M.
Mukhin, K.
Hernandez-Hernandez, L.
Maher, B.
Sisodiya, S.
Kuhn, M.
Glaeser, D.
Wechuysen, S.
Myers, C. T.
Mefford, H. C.
Hortnagel, K.
Biskup, S.
Lemke, J. R.
Heron, D.
Kluger, G.
Depienne, C.
机构：
来源：
JOURNAL OF MEDICAL GENETICS | 2016年 / 53卷 / 10期
关键词：
D O I：
10.1136/jmedgenet-2015-103451corr1
中图分类号：
Q3 [遗传学];
学科分类号：
071007 ; 090102 ;
摘要：
引用
收藏
页码：720 / 720
页数：1
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