BRPF1‐associated intellectual disability, ptosis, and facial dysmorphism in a multiplex family

BACKGROUND: Over 500 epigenetic regulators have been identified throughout the human genome. Of these, approximately 30 chromatin modifiers have been implicated thus far in human disease. Recently, variants in BRPF1, encoding a chromatin reader, have been associated with a previously unrecognized au...

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Detalles Bibliográficos
Autores principales: Pode‐Shakked, Naomi, Barel, Ortal, Pode‐Shakked, Ben, Eliyahu, Aviva, Singer, Amihood, Nayshool, Omri, Kol, Nitzan, Raas‐Rothschild, Annick, Pras, Elon, Shohat, Mordechai
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2019
Materias:
Original Articles
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6565580/
https://www.ncbi.nlm.nih.gov/pubmed/31020800
http://dx.doi.org/10.1002/mgg3.665

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6565580/
https://www.ncbi.nlm.nih.gov/pubmed/31020800
http://dx.doi.org/10.1002/mgg3.665

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