Rett syndrome linked to defects in forming the MeCP2/Rbfox/LASR complex in mouse models
Rett syndrome linked to defects in forming the MeCP2/Rbfox/LASR complex in mouse models
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Author / Creator
Jiang, Yan , Fu, Xing , Zhang, Yuhan , Wang, Shen-Fei , Zhu, Hong , Wang, Wei-Kang , Zhang, Lin , Wu, Ping , Wong, Catherine C. L. , Li, Jinsong , Ma, Jinbiao , Guan, Ji-Song , Huang, Ying and Hui, Jingyi
Publisher
London: Nature Publishing Group UK
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Language
English
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Publisher
London: Nature Publishing Group UK
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Contents
Rett syndrome (RTT) is a severe neurological disorder and a leading cause of intellectual disability in young females. RTT is mainly caused by mutations found in the X-linked gene encoding methyl-CpG binding protein 2 (MeCP2). Despite extensive studies, the molecular mechanism underlying RTT pathogenesis is still poorly understood. Here, we report...
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Full title
Rett syndrome linked to defects in forming the MeCP2/Rbfox/LASR complex in mouse models
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Record Identifier
TN_cdi_doaj_primary_oai_doaj_org_article_fa106e341c1247a4a340882447b44d12
Permalink
https://devfeature-collection.sl.nsw.gov.au/record/TN_cdi_doaj_primary_oai_doaj_org_article_fa106e341c1247a4a340882447b44d12
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ISSN
2041-1723
E-ISSN
2041-1723
DOI
10.1038/s41467-021-26084-3
