De novo variants in ATP2B1 lead to neurodevelopmental delay.

Rahimi MJ, Urban N, Wegler M, Sticht H, Schaefer M, Popp B, Gaunitz F, Morleo M, Nigro V, Maitz S, Mancini GM, Ruivenkamp C, Suk EK, Bartolomaeus T, Merkenschlager A, Koboldt D, Bartholomew D, Stegmann AP, Sinnema M, Duynisveld I, Salvarinova R, Race S, de Vries BB, Trimouille A, Naudion S, Marom D, Hamiel U, Henig N, Demurger F, Rahner N, Bartels E, Hamm JA, Putnam AM, Person R, Jamra RA, Oppermann H (2025)


Publication Type: Journal article, Erratum

Publication year: 2025

Journal

Book Volume: 112

Pages Range: 3046-3047

Journal Issue: 12

DOI: 10.1016/j.ajhg.2025.10.017

How to cite

APA:

Rahimi, M.J., Urban, N., Wegler, M., Sticht, H., Schaefer, M., Popp, B.,... Oppermann, H. (2025). De novo variants in ATP2B1 lead to neurodevelopmental delay. American Journal of Human Genetics, 112(12), 3046-3047. https://doi.org/10.1016/j.ajhg.2025.10.017

MLA:

Rahimi, Meer Jacob, et al. "De novo variants in ATP2B1 lead to neurodevelopmental delay." American Journal of Human Genetics 112.12 (2025): 3046-3047.

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