Epigenomic and transcriptomic signatures of a Klinefelter syndrome (47,XXY) karyotype in the brain

Klinefelter syndrome (KS) is the most common sex-chromosome aneuploidy in humans. Most affected individuals carry one extra X-chromosome (47,XXY karyotype) and the condition presents with a heterogeneous mix of reproductive, physical and psychiatric phenotypes. Although the mechanism(s) by which the...

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Detalhes bibliográficos
Main Authors: Viana, Joana, Pidsley, Ruth, Troakes, Claire, Spiers, Helen, Wong, Chloe CY, Al-Sarraj, Safa, Craig, Ian, Schalkwyk, Leonard, Mill, Jonathan
Formato: Artigo
Idioma:Inglês
Publicado em: Landes Bioscience 2014
Assuntos:
Research Paper
Acesso em linha:https://ncbi.nlm.nih.gov/pmc/articles/PMC4121369/
https://ncbi.nlm.nih.gov/pubmed/24476718
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.4161/epi.27806
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