Cite
MLA Citation
Amber Geerts‐Haages et al.. “A novel UBE3A sequence variant identified in eight related individuals with neurodevelopmental delay, results in a phenotype which does not match the clinical criteria of Angelman syndrome.” Molecular genetics & genomic medicine, vol. 8, no. 11, 2020, p. n/a. http://access.bl.uk/ark:/81055/vdc_100119957824.0x00000c