Updated insight into the mutational and phenotypic spectrum of MED13L-related intellectual disability - Asadollahi, R.; Boonsawat, P.; Popp, B.; Torti, E.; Bader, I.; Vitobello, A.; Moutton, S.; Pinson, L.; Lambert, L.; Thuresson, A. C.; Sobol, M.; Zander, C. Soussi; et al. (EUROPEAN JOURNAL OF HUMAN GENETICS, 2020)
CRIS-Team WoS Importer:2021-01-22