Genetic interaction screen for severe neurodevelopmental disorders reveals a functional link between Ube3a and Mef2 in Drosophila melanogaster

Neurodevelopmental disorders (NDDs) are clinically and genetically extremely heterogeneous with shared phenotypes often associated with genes from the same networks. Mutations in TCF4, MEF2C, UBE3A, ZEB2 or ATRX cause phenotypically overlapping, syndromic forms of NDDs with severe intellectual disab...

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Detalles Bibliográficos
Autores principales: Straub, Jonas, Gregor, Anne, Sauerer, Tatjana, Fliedner, Anna, Distel, Laila, Suchy, Christine, Ekici, Arif B., Ferrazzi, Fulvia, Zweier, Christiane
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2020
Materias:
Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6985129/
https://www.ncbi.nlm.nih.gov/pubmed/31988313
http://dx.doi.org/10.1038/s41598-020-58182-5

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6985129/
https://www.ncbi.nlm.nih.gov/pubmed/31988313
http://dx.doi.org/10.1038/s41598-020-58182-5

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