The defining DNA methylation signature of Floating-Harbor Syndrome

Floating-Harbor syndrome (FHS) is an autosomal dominant genetic condition characterized by short stature, delayed osseous maturation, expressive language impairment, and unique facial dysmorphology. We previously identified mutations in the chromatin remodeling protein SRCAP (SNF2-related CBP Activa...

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Detalles Bibliográficos
Autores principales: Hood, Rebecca L., Schenkel, Laila C., Nikkel, Sarah M., Ainsworth, Peter J., Pare, Guillaume, Boycott, Kym M., Bulman, Dennis E., Sadikovic, Bekim
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group 2016
Materias:
Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5146968/
https://www.ncbi.nlm.nih.gov/pubmed/27934915
http://dx.doi.org/10.1038/srep38803

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5146968/
https://www.ncbi.nlm.nih.gov/pubmed/27934915
http://dx.doi.org/10.1038/srep38803

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