DNA methylation signature associated with Bohring-Opitz syndrome: a new tool for functional classification of variants in ASXL genes

The additional sex combs-like (ASXL) gene family—encoded by ASXL1, ASXL2, and ASXL3—is crucial for mammalian development. Pathogenic variants in the ASXL gene family are associated with three phenotypically distinct neurodevelopmental syndromes. Our previous work has shown that syndromic conditions...

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Detalles Bibliográficos
Autores principales: Awamleh, Zain, Chater-Diehl, Eric, Choufani, Sanaa, Wei, Elizabeth, Kianmahd, Rebecca R., Yu, Anna, Chad, Lauren, Costain, Gregory, Tan, Wen-Hann, Scherer, Stephen W., Arboleda, Valerie A., Russell, Bianca E., Weksberg, Rosanna
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Springer International Publishing 2022
Materias:
Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9177544/
https://www.ncbi.nlm.nih.gov/pubmed/35361921
http://dx.doi.org/10.1038/s41431-022-01083-0

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9177544/
https://www.ncbi.nlm.nih.gov/pubmed/35361921
http://dx.doi.org/10.1038/s41431-022-01083-0

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