O'Brien, Margaret M.

Clinical spectrum and genotype–phenotype associations of KCNA2-related encephalopathies

Masnada, Silvia , Gardella, Elena , Schubert, Julian , Kaiwar, Charu , Klee, Eric W. , Lanpher, Brendan C. , Gavrilova, Ralitza H. , Synofzik, Matthis , Bast, Thomas , Gorman, Kathleen M. , King, Mary D. , Allen, Nicholas M. , Conroy, Judith, Zeev, Bruria Ben , Tzadok, Michal , Korff, Christian , Dubois, Fanny, Ramsey, Keri , Serratosa, José M. , Giráldez, Beatriz G. , Bergqvist, Christina A , Binelli, Adrian , Zaeyen, Eduardo José Bernardo, Wolff, Markus , Marjanović, Dragan , Çağlayan, Hande, Pena, Sérgio D.J. , Balestrini, Simona , Syrbe, Steffen , Møller, Rikke S. , Rubboli, Guido , Hedrich, Ulrike B. S. , Narayanan, Vinodh , Helbig, Ingo , Marsh, Eric D. , O'Brien, Margaret M. , Porter, Brenda E. , Horovitz, Dafne Dain Gandelman , Arslan, Mutluay , Sisodiya, Sanjay , Veggiotti, Pierangelo , Lemke, Johannes R. , Lerche, Holger , Serratosa, José M , Gorman, Kathleen M , Rubboli, Guido , Synofzik, Matthis , Balestrini, Simona , Gardella, Elena , Møller, Rikke S

Brain | June 29, 2017 | Volume: 140 | Issue: 9 | Pages: 2337-2354

10.1093/brain/awx184