Cite
MLA Citation
Julien Buratti et al.. “De novo variants in SIAH1, encoding an E3 ubiquitin ligase, are associated with developmental delay, hypotonia and dysmorphic features.” Journal of medical genetics, vol. 58, no. 3, 2021, pp. 205–212. http://access.bl.uk/ark:/81055/vdc_100174257022.0x000054