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...
Gorde:
| Egile Nagusiak: | , , , , , , , , |
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| Formatua: | Artigo |
| Hizkuntza: | ingelesa |
| Argitaratua: |
2014
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| Sarrera elektronikoa: | https://doi.org/10.4161/epi.27806 https://www.tandfonline.com/doi/pdf/10.4161/epi.27806?needAccess=true |
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