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Multi-modal investigation reveals pathogenic features of diverse DDX3X missense mutations.

De novo mutations in the RNA binding protein DDX3X cause neurodevelopmental disorders including DDX3X syndrome and autism spectrum disorder. Amongst ~200 mutations identified to date, half are missense. While DDX3X loss of function is known to impair neural cell fate, how the landscape of missense m...

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I tiakina i:
Ngā taipitopito rārangi puna kōrero
Ngā kaituhi matua: Federica Mosti, Mariah L Hoye, Carla F Escobar-Tomlienovich, Debra L Silver
Hōputu: Artigo
Reo:Inglês
I whakaputaina: Public Library of Science (PLoS) 2025-01-01
Rangatū:PLoS Genetics
Urunga tuihono:https://doi.org/10.1371/journal.pgen.1011555
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