Euchromatin histone methyltransferase 1 regulates cortical neuronal network development

Heterozygous mutations or deletions in the human Euchromatin histone methyltransferase 1 (EHMT1) gene cause Kleefstra syndrome, a neurodevelopmental disorder that is characterized by autistic-like features and severe intellectual disability (ID). Neurodevelopmental disorders including ID and autism...

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Detalles Bibliográficos
Autores principales: Bart Martens, Marijn, Frega, Monica, Classen, Jessica, Epping, Lisa, Bijvank, Elske, Benevento, Marco, van Bokhoven, Hans, Tiesinga, Paul, Schubert, Dirk, Nadif Kasri, Nael
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group 2016
Materias:
Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5073331/
https://www.ncbi.nlm.nih.gov/pubmed/27767173
http://dx.doi.org/10.1038/srep35756

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5073331/
https://www.ncbi.nlm.nih.gov/pubmed/27767173
http://dx.doi.org/10.1038/srep35756

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