A homozygous human WNT11 loss-of-function variant associated with laterality, heart and renal defects
Henrike Berns, Maximilian Haas, Zeineb Bakey, Magdalena Maria Brislinger-Engelhardt, Miriam Schmidts, Peter Walentek
The paper identifies a homozygous WNT11 variant causing laterality, heart, and renal defects in an infant and shows its loss-of-function in Xenopus embryos.
bioRxiv · Nov 14, 2024 · PreprintDevelopmental Biology