Cite
MLA Citation
Stijn N V Bossuyt et al.. “Loss of nuclear UBE3A activity is the predominant cause of Angelman syndrome in individuals carrying UBE3A missense mutations.” Human molecular genetics, vol. 30, no. 6, 2021, pp. 430–442. http://access.bl.uk/ark:/81055/vdc_100129565666.0x00001a