X-Chromosome Inactivation in Rett Syndrome Human Induced Pluripotent Stem Cells

Rett syndrome (RTT) is a neurodevelopmental disorder that affects girls due primarily to heterozygous mutations in the X-linked gene encoding methyl-CpG binding protein 2 (MECP2). Random X-chromosome inactivation (XCI) results in cellular mosaicism in which some cells express wild-type (WT) MECP2 wh...

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Autors principals: Cheung, Aaron Y. L., Horvath, Lindsay M., Carrel, Laura, Ellis, James
Format: Artigo
Idioma:Inglês
Publicat: Frontiers Research Foundation 2012
Matèries:
Psychiatry
Accés en línia:https://ncbi.nlm.nih.gov/pmc/articles/PMC3311266/
https://ncbi.nlm.nih.gov/pubmed/22470355
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.3389/fpsyt.2012.00024
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