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

被引：0
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作者：
Ainhoa Pascual-Alonso
Clara Xiol
Dmitrii Smirnov
Robert Kopajtich
Holger Prokisch
Judith Armstrong
机构：
[1] Fundació Per La Recerca Sant Joan de Déu,Institute of Human Genetics
[2] Institut de Recerca Sant Joan de Déu,Institute of Neurogenomics
[3] Technical University of Munich,CIBER
[4] Helmholtz Zentrum München,ER (Biomedical Network Research Center for Rare Diseases)
[5] Instituto de Salud Carlos III (ISCIII),Genomic Unit, Molecular and Genetic Medicine Section
[6] Hospital Sant Joan de Déu,undefined
来源：
Human Genomics | / 17卷
关键词：
Rett syndrome; MECP2 duplication syndrome; Rett-like phenotypes; Multi-omics; Transcriptomics; Proteomics; Differential expression;
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