A Novel Homozygous PDE 10A Variant Leading to Infantile-Onset Hyperkinesia

被引：1

作者：

Trieschmann, Gesa ^{[1
]}

Wach, Katharina ^{[1
,2
]}

Abel, Maria ^{[3
]}

Tilgner, Eva ^{[4
]}

Berweck, Steffen ^{[1
,5
]}

Zech, Michael ^{[6
,7
]}

机构：

[1] Schoen Clin Vogtareuth, Specialist Ctr Paediat Neurol Neurorehabil & Epil, Krankenhausstr 20, D-83569 Vogtareuth, Bayern, Germany

[2] Univ Hosp Gottingen, Dept Paediat, Gottingen, Germany

[3] Specialist Ctr Neurosurg & Epilepsy Surg, Vogtareuth, Bayern, Germany

[4] DONAUISAR Klinikum Deggendorf, Social Paediat Ctr, Deggendorf, Germany

[5] Ludwig Maximilians Univ Munchen, LMU Hosp, Div Pediat Neurol & Dev Med, Dept Pediat,Dr von Hauner Childrenss Hosp, Munich, Germany

[6] Tech Univ Munich, Inst Human Genet, Sch Med, Munich, Germany

[7] Helmholtz Zentrum Munchen, Inst Neurogen, Munich, Neuherberg, Germany

来源：

关键词：

MUTATIONS;

D O I：

10.1055/a-1892-1547

中图分类号：

R74 [神经病学与精神病学];

学科分类号：

摘要：

引用

页码：386 / 387

页数：2