SWI/SNF complex in disorder: SWItching from malignancies to intellectual disability

Heterozygous germline mutations in components of switch/sucrose nonfermenting (SWI/SNF) chromatin remodeling complexes were recently identified in patients with non-syndromic intellectual disability, Coffin-Siris syndrome and Nicolaides-Baraitser syndrome. The common denominator of the phenotype of...

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Detalles Bibliográficos
Autores principales: Santen, Gijs W.E., Kriek, Marjolein, van Attikum, Haico
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Landes Bioscience 2012
Materias:
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Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3499322/
https://www.ncbi.nlm.nih.gov/pubmed/23010866
http://dx.doi.org/10.4161/epi.22299

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3499322/
https://www.ncbi.nlm.nih.gov/pubmed/23010866
http://dx.doi.org/10.4161/epi.22299

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