Identification of a novel CDKL5 exon and pathogenic mutations in patients with severe mental retardation, early-onset seizures and Rett-like features

被引:0
作者
Nils Rademacher
Melanie Hambrock
Ute Fischer
Bettina Moser
Berten Ceulemans
Wolfgang Lieb
Rainer Boor
Irina Stefanova
Gabriele Gillessen-Kaesbach
Charlotte Runge
Georg Christoph Korenke
Stefanie Spranger
Franco Laccone
Andreas Tzschach
Vera M. Kalscheuer
机构
[1] Department of Human Molecular Genetics,Max Planck Institute for Molecular Genetics
[2] University of Antwerp,Department of Neurology
[3] Universität zu Lübeck,Child Neurology
[4] Universitätsklinikum Schleswig-Holstein,Institut für Humangenetik
[5] Campus,Klinik für Neuropädiatrie
[6] Children’s Hospital,Department of Neuropediatrics
[7] Praxis für Humangenetik,Department of Medical Genetics
[8] Medical University of Vienna,undefined
来源
neurogenetics | 2011年 / 12卷
关键词
CDKL5; Rett syndrome; Seizures; Infantile spasms;
D O I
暂无
中图分类号
学科分类号
摘要
引用
收藏
页码:165 / 167
页数:2
相关论文
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Menzel C(undefined)CDKL5 influences RNA splicing activity by its association to the nuclear speckle molecular machinery undefined undefined undefined-undefined
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Hoeltzenbein M(undefined)An isoform of the severe encephalopathy-related undefined undefined undefined-undefined
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Tommerup N(undefined) gene, including a novel exon with extremely high sequence conservation, is specifically expressed in brain undefined undefined undefined-undefined
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Eyre H(undefined)undefined undefined undefined undefined-undefined