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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.
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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  Data: A recurrent mutation in KCNA2 as a novel cause of hereditary spastic paraplegia and ataxia.
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  Data: <searchLink fieldCode="JN" term="%22Annals+of+Neurology%22">Annals of Neurology</searchLink>. Oct2016, Vol. 80 Issue 4, pn/a-N.PAG. 5p.
PLink https://search.ebscohost.com/login.aspx?direct=true&site=eds-live&db=asn&AN=118369913
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