Compromised genomic integrity impedes muscle growth after Atrx inactivation

ATR-X syndrome is a severe intellectual disability disorder caused by mutations in the ATRX gene. Many ancillary clinical features are attributed to CNS deficiencies, yet most patients have muscle hypotonia, delayed ambulation, or kyphosis, pointing to an underlying skeletal muscle defect. Here, we...

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Detaylı Bibliyografya
Asıl Yazarlar: Huh, Michael S., Price O’Dea, Tina, Ouazia, Dahmane, McKay, Bruce C., Parise, Gianni, Parks, Robin J., Rudnicki, Michael A., Picketts, David J.
Materyal Türü: Artigo
Dil:Inglês
Baskı/Yayın Bilgisi: American Society for Clinical Investigation 2012
Konular:
Research Article
Online Erişim:https://ncbi.nlm.nih.gov/pmc/articles/PMC3533543/
https://ncbi.nlm.nih.gov/pubmed/23114596
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1172/JCI63765
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