Cite
HARVARD Citation
Penon‐Portmann, M. et al. (2022). De novo heterozygous variants in SLC30A7 are a candidate cause for Joubert syndrome. American journal of medical genetics. 188 (8), pp. 2360-2366. [Online].
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Penon‐Portmann, M. et al. (2022). De novo heterozygous variants in SLC30A7 are a candidate cause for Joubert syndrome. American journal of medical genetics. 188 (8), pp. 2360-2366. [Online].