De novo ARX mutations in female patients with agenesis of the corpus callosum and intellectual disability

被引：0

作者：

Taveira, M. ^{[1
]}

Heide, S. ^{[2
]}

Mignot, C. ^{[2
]}

Milh, M. ^{[3
]}

Rastetter, A. ^{[4
]}

Jacquette, A. ^{[2
]}

Charles, P. ^{[2
]}

Marey, I. ^{[2
]}

Whalen, S. ^{[1
]}

Keren, B. ^{[5
]}

Nava, C. ^{[5
]}

Heron, D. ^{[2
]}

机构：

[1] Hop Armand Trousseau, APHP, UF Genet Clin, Paris, France

[2] GH Pitie Salpetriere, APHP, Dept Genet, UF Genet Med,Ctr Reference Deficiences Intellectu, Paris, France

[3] Hop La Timone, APHM, Serv Neuropediat, Marseille, France

[4] UPMC, INSERM, UMR S975, CNRS,UMR 7225,ICM, Paris, France

[5] GH Pitie Salpetriere, Dept Genet, UF Genom Dev, Paris, France

来源：

EUROPEAN JOURNAL OF HUMAN GENETICS | 2018年 / 26卷

关键词：

D O I：

暂无

中图分类号：

Q5 [生物化学]; Q7 [分子生物学];

学科分类号：

071010 ; 081704 ;

摘要：

P08.07C

引用

页码：327 / 328

页数：2

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