Article Dans Une Revue American Journal of Medical Genetics Part A Année : 2021

Syndromic neurodevelopmental disorder associated with de novo variants in DDX23

Neda Zadeh
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Michael J Lyons
  • Fonction : Auteur
  • PersonId : 1101322

Résumé

The DEAD/DEAH box RNA helicases are a superfamily of proteins involved in the processing and transportation of RNA within the cell. A growing literature supports this family of proteins as contributing to various types of human disorders from neurodevelopmental disorders to syndromes with multiple congenital anomalies. This article presents a cohort of nine unrelated individuals with de novo missense alterations in DDX23 (Dead-Box Helicase 23). The gene is ubiquitously expressed and functions in RNA splicing, maintenance of genome stability, and the sensing of double-stranded RNA. Our cohort of patients, gathered through GeneMatcher, exhibited features including tone abnormalities, global developmental delay, facial

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Génétique
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Dates et versions

hal-03251630 , version 1 (07-06-2021)

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William Burns, Lynne M Bird, Delphine Heron, Boris Keren, Divya Ramachandra, et al.. Syndromic neurodevelopmental disorder associated with de novo variants in DDX23. American Journal of Medical Genetics Part A, 2021, ⟨10.1002/ajmg.a.62359⟩. ⟨hal-03251630⟩
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