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X-Chromosome Inactivation Patterns Are Unbalanced and Affect the Phenotypic Outcome in a Mouse Model of Rett Syndrome

Rett syndrome (RTT), a neurodevelopmental disorder affecting mostly females, is caused by mutations in the X-linked gene encoding methyl-CpG–binding protein 2 (MeCP2). Although the majority of girls with classic RTT have a random pattern of X-chromosome inactivation (XCI), nonbalanced patterns have...

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Detaylı Bibliyografya
Asıl Yazarlar: Young, Juan I., Zoghbi, Huda Y.
Materyal Türü: Artigo
Dil:Inglês
Baskı/Yayın Bilgisi: The American Society of Human Genetics 2004
Konular:
Online Erişim:https://ncbi.nlm.nih.gov/pmc/articles/PMC1182264/
https://ncbi.nlm.nih.gov/pubmed/14973779
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