Adaptor protein 2 sigma subunit (AP2S1) variants associated with neurodevelopmental disorders

Stevenson M., Bayliss A., Stokes V., English K., Kooblall K., Fischer R., Heilig R., Vendrell I., Albers M., Bartos M., Begtrup A., Bourgois A., Buchert R., Carey D., Carere D., Carnevale A., Claeys K., Cogne B., Costain G., de Leeuw N., Denommé-Pichon A-S., Donner E., Drogouti E., Dyment D., Gangaram B., Haack T., Haley J., Heide S., Husain R., Isidor B., Izatt L., Jacquinet A., Juusola J., Kahle J., Keren B., Klee E., Kokosali E., Lanpher B., Macke E., Marco E., McWalter K., Mendelsohn B., Milunsky A., Osmond M., Piton A., Riess A., Ruault V., Rump P., Schuhmann S., Shillington A., Smelser D., Snijders Blok L., Tran Mau-Them F., Tsakalidis C., Turnwald A., Van Gassen K., Van Schil K., Vasileiou G., Vawter-Lee M., Willems M., Willemsen M., Wong-Kisiel L., Wonneberger A., Zaganas I., Genomics England Research Consortium ., Hannan F., Lines K., Thakker R.

DOI

10.1101/2024.07.22.24310683

Type

Preprint

Publication Date

2024-01-01T00:00:00+00:00

Keywords

Genomics England Research Consortium

Permalink More information Close