Cite
MLA Citation
Monica Penon‐Portmann et al.. “De novo heterozygous variants in SLC30A7 are a candidate cause for Joubert syndrome.” American journal of medical genetics, vol. 188, no. 8, 2022, pp. 2360–2366. http://access.bl.uk/ark:/81055/vdc_100159484883.0x00001f