Neurodevelopmental Disorders Caused by Defective Chromatin Remodeling: Phenotypic Complexity Is Highlighted by a Review of ATRX Function

The ability to determine the genetic etiology of intellectual disability (ID) and neurodevelopmental disorders (NDD) has improved immensely over the last decade. One prevailing metric from these studies is the large percentage of genes encoding epigenetic regulators, including many members of the AT...

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Detalles Bibliográficos
Autores principales: Timpano, Sara, Picketts, David J.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2020
Materias:
Genetics
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7432156/
https://www.ncbi.nlm.nih.gov/pubmed/32849845
http://dx.doi.org/10.3389/fgene.2020.00885

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7432156/
https://www.ncbi.nlm.nih.gov/pubmed/32849845
http://dx.doi.org/10.3389/fgene.2020.00885

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