A recurrent mutation in KCNA2 as a novel cause of hereditary spastic paraplegia and ataxia.

Added 1925 days ago (21.08.2016)
Authors: Helbig KL, Hedrich UB, Shinde DN, Krey I, Teichmann AC, Hentschel J, Schubert J, Chamberlin AC, Huether R, Lu HM, Alcaraz WA, Tang S, Jungbluth C, Dugan SL, Vainionpää L, Karle KN, Synofzik M, Schöls L, Schüle R, Lehesjoki AE, Helbig I, Lerche H, Lemke JR
PubMed id: 27543892
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