A recurrent mutation in KCNA2...

Annals of Neurology 2016 / 08

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

Helbig, Katherine L., Hedrich, Ulrike B. S., Shinde, Deepali N., Krey, Ilona, Teichmann, Anne-Christin, Hentschel, Julia, Schubert, Julian, Chamberlin, Adam C., Huether, Robert, Lu, Hsiao-Mei, Alcaraz
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Language:
english
Journal:
Annals of Neurology
DOI:
10.1002/ana.24762
Date:
August, 2016
File:
PDF, 1.32 MB
english, 2016
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