Familial cortical myoclonus with a mutation in NOL3.
Russell JF; Steckley JL; Coppola G; Hahn AF; Howard MA; Kornberg Z; Huang A; Mirsattari SM; Merriman B; Klein E; Choi M; Lee HY; Kirk A; Nelson-Williams C; Gibson G; Baraban SC; Lifton RP; Geschwind DH; Fu YH; Ptáček LJ; Annals Of Neurology, 2012, vol. 72, issue 2, p 175, ISSN 15318249. ISBN 15318249.

Full Text Resources Located for this Citation

View article on EBSCOhost(Login required)
View article via CrossRef