De novo MECP2 mutation in a 46,XX male patient with Rett syndrome

被引：0
|
作者：
Robert Maiwald
Anselm Bönte
Helena Jung
Pavel Bitter
Zoe Storm
Franco Laccone
Peter Herkenrath
机构：
[1] Institute of Medical Genetics and Molecular Medicine,
[2] Paul-Schalluck-Strasse 8,undefined
[3] 50939 Cologne,undefined
[4] Germany,undefined
[5] Children's Hospital,undefined
[6] University of Cologne,undefined
[7] Joseph-Stelzmann-Strasse 9,undefined
[8] 50924 Cologne,undefined
[9] Germany,undefined
[10] Institute of Human Genetics,undefined
[11] University of Göttingen,undefined
[12] Heinrich-Düker-Weg 12,undefined
[13] 37073 Göttingen,undefined
[14] Germany,undefined
来源：
Neurogenetics | 2002年 / 4卷
关键词：
Rett syndrome MECP2 E455X XX male;
D O I：
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摘要：
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页码：107 / 108
页数：1
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