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...

Full beskrivning

Sparad:
Bibliografiska uppgifter
I publikationen:Mol Genet Genomic Med
Huvudupphovsmän: Pode‐Shakked, Naomi, Barel, Ortal, Pode‐Shakked, Ben, Eliyahu, Aviva, Singer, Amihood, Nayshool, Omri, Kol, Nitzan, Raas‐Rothschild, Annick, Pras, Elon, Shohat, Mordechai
Materialtyp: Artigo
Språk:Inglês
Publicerad: John Wiley and Sons Inc. 2019
Ämnen:
Original Articles
Länkar:https://ncbi.nlm.nih.gov/pmc/articles/PMC6565580/
https://ncbi.nlm.nih.gov/pubmed/31020800
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1002/mgg3.665
Taggar: Lägg till en tagg
Inga taggar, Lägg till första taggen!

Liknande verk