Effect of Humanizing Mutations on the Stability of the Llama Single-Domain Variable RegionMiguel A. Soler, Ario de Marco, Sara Fortuna et al.|Biomolecules|2021Cited by 28
De novo <i>KCNA6</i> variants with attenuated <scp>K<sub>V</sub></scp>1.6 channel deactivation in patients with epilepsyVincenzo Salpietro, Roope Männikkö, Valentina Galassi Deforie et al.|Epilepsia|2022Cited by 18
Genotype–phenotype correlations and disease mechanisms in PEX13-related Zellweger spectrum disordersPaola Borgia, Vincenzo Salpietro, Sımona Baldassari et al.|Orphanet Journal of Rare Diseases|2022Cited by 5