A recurrent mutation in KCNA2 as a novel cause of hereditary spastic paraplegia and ataxia.
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| Title: | A recurrent mutation in KCNA2 as a novel cause of hereditary spastic paraplegia and ataxia. |
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| Authors: | Helbig, Katherine L.1, Hedrich, Ulrike B.S.2, Shinde, Deepali N.1, Krey, Ilona3, Teichmann, Anne‐Christin3, Hentschel, Julia3, Schubert, Julian2, Chamberlin, Adam C.4, Huether, Robert4, Lu, Hsiao‐Mei4, Alcaraz, Wendy A.1, Tang, Sha1, Jungbluth, Chelsy5, Dugan, Sarah L.5,6, Vainionpää, Leena7, Karle, Kathrin N.8,9,10, Synofzik, Matthis8,9, Schöls, Ludger8,9, Schüle, Rebecca8,9, Lehesjoki, Anna‐Elina11 |
| Source: | Annals of Neurology. Oct2016, Vol. 80 Issue 4, pn/a-N.PAG. 5p. |
| Database: | Academic Search Ultimate |
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