← Evidence map

ArticleBrain : a journal of neurology2025

De novo and inherited variants in DDX39B cause a novel neurodevelopmental syndrome.

Kevin T A Booth et al.PubMed ↗Full text ↗Publisher ↗

No numbers read from the abstract.

7 papers cite it

2025
2026
this papercites it
Full record →Abstract, authors, funding and every citing paper · PMID 39918047