Mutations in PTPN11 could lead to a congenital myasthenic syndrome phenotype: a Noonan syndrome case series - Pugliese, Alessia; Marina, Adela Della; Estephan, Eduardo de Paula; Zanoteli, Edmar; Roos, Andreas; Schara-Schmidt, Ulrike; Hentschel, Andreas; Azuma, Yoshiteru; Topf, Ana; Thompson, Rachel (JOURNAL OF NEUROLOGY, 2024)