Bi-allelic truncating mutations in VWA1 cause neuromyopathy - Deschauer, Marcus; Hengel, Holger; Rupprich, Katrin; Kreiß, Martina; Schlotter-Weigel, Beate; Grimmel, Mona; Admard, Jakob; Schneider, Ilka; Alhaddad, Bader; Gazou, Anastasia; Sturm, Marc; Vorgerd, Matthias; et al. (Brain, 2021)
Gesehen am 22.02.2022