De novo heterozygous variants of the RSF1 gene are responsible for a syndromic neurodevelopmental disorder
Céline Jost(Maison des Sciences sociales et des Humanités de Dijon), L. Faivre(Inserm)
Cited by 1
Related Papers
ARID1B-related disorder in 87 adults: Natural history and self-sustainability
|Genetics in Medicine Open|2024|6
Tyrosine kinase inhibitors in Kosaki/Penttinen syndromes: new reports, follow-up of treated individuals and literature review
|European Journal of Human Genetics|2026|0