LOSS-OF-FUNCTION VARIANTS IN CUL3 CAUSE A SYNDROMIC NEURODEVELOPMENTAL DISORDER

被引：0

作者：

Wang, Tianyun ^{[1
]}

Blackburn, Patrick ^{[2
]}

Ebstein, Frederic ^{[3
]}

Hsieh, Tzung-Chien ^{[4
]}

Motta, Marialetizia ^{[5
]}

Radio, Francesca Clementina ^{[5
]}

Herkert, Johanna ^{[6
]}

Rinne, Tuula ^{[7
]}

Krueger, Elke ^{[3
]}

Bezieau, Stephane ^{[8
]}

Klinkhammer, Hannah ^{[4
]}

Krawitz, Peter Michael ^{[8
]}

Eichler, Evan ^{[9
]}

Tartaglia, Marco ^{[5
]}

Kuery, Sebastien ^{[8
]}

机构：

[1] Peking Univ, Hlth Sci Ctr, Ctr Med Genet, Beijing, Peoples R China

[2] St Jude Childrens Res Hosp, Memphis, TN USA

[3] Univ Med Greifswald, Inst Med Biochem & Mol Biol, Greifswald, Germany

[4] Univ Bonn, Inst Genom Stat & Bioinformat, Bonn, Germany

[5] IRCCS, Osped Pediat Bambino Gesu, Mol Genet & Funct Gen, Rome, Italy

[6] Univ Groningen, Univ Med Ctr Groningen, Groningen, Netherlands

[7] Radboud Univ Nijmegen, Med Ctr, Nijmegen, Netherlands

[8] Nantes Univ, CNRS, CHU Nantes, INSERM,Inst Thorax, Nantes, France

[9] Univ Washington, Sch Med, Seattle, WA USA

来源：

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D O I：

暂无

中图分类号：

R74 [神经病学与精神病学];

学科分类号：

摘要：

F55

引用

页码：235 / 235

页数：1