A recurrent mutation in KCNA2 in complicated autosomal dominant spastic paraplegia: An expansion of the channelopathy spectrum and a novel disease mechanism
Title: A recurrent mutation in KCNA2 in complicated autosomal dominant spastic paraplegia: An expansion of the channelopathy spectrum and a novel disease mechanism
Speakers: K.L. Helbig; U.B.S. Hedrich; A.C. Teichmann; J. Hentschel; D.N. Shinde; W.A. Alcaraz; S. Tang; C. Jungbluth; S.L. Dugan; R. Schüle; H. Lerche; J.R. Lemke