Identification of molecular signatures and pathways involved in Rett syndrome-spectrum disorders using a multi-omics approach

被引：0
|
作者：
Xiol, Clara [1 ,2 ]
Pascual-Alonso, Ainhoa [1 ,2 ]
Smirnov, Dmitrii [3 ,4 ]
Kopajtich, Robert [3 ,4 ]
Ludwig, Christina [5 ]
Prokisch, Holger [3 ,4 ]
Armstrong, Judith [2 ,6 ,7 ]
机构：
[1] Fundacio Recerca Sant Joan Deu, Esplugas de Llobregat, Spain
[2] Inst Recerca Sant Joan Deu, Esplugas de Llobregat, Spain
[3] Tech Univ Munich, Inst Human Genet, Munich, Germany
[4] Helmholtz Zentrum Munchen, Inst Neurogen, Munich, Germany
[5] Tech Univ Munich, Bavarian Biomol Mass Spect Ctr, Freising Weihenstephan, Germany
[6] Inst Salud Carlos III ISCIII, CIBER ER Biomed Network Res Ctr Rare Dis, Madrid, Spain
[7] Hosp San Juan Dios, Mol & Genet Med Sect, Genom Unit, Barcelona, Spain
来源：
EUROPEAN JOURNAL OF HUMAN GENETICS | 2023年 / 31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：
P10.079.B
引用
收藏
页码：496 / 496
页数：1
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