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BETting on a Transcriptional Deficit as the Main Cause for Cornelia de Lange Syndrome

Cornelia de Lange Syndrome (CdLS) is a human developmental syndrome with complex multisystem phenotypic features. It has been traditionally considered a cohesinopathy together with other phenotypically related diseases because of their association with mutations in subunits of the cohesin complex. D...

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Detalles Bibliográficos
Autores principales:	García-Gutiérrez, Pablo, García-Domínguez, Mario
Formato:	Online Artículo Texto
Lenguaje:	English
Publicado:	Frontiers Media S.A. 2021
Materias:	Molecular Biosciences
Acceso en línea:	https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8353280/ https://www.ncbi.nlm.nih.gov/pubmed/34386522 http://dx.doi.org/10.3389/fmolb.2021.709232

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