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1. De novo KCNA2 mutations cause hereditary spastic paraplegia.

Author

Manole, Andreea, Männikkö, Roope, Hanna, Michael G., Kullmann, Dimitri M., Houlden, Henry, Männikkö, Roope, and SYNAPS study group

Abstract

A letter to the editor is presented in response to the article "A recurrent mutation in KCNA2 as a novel cause of hereditary spastic paraplegia and ataxia" by K.L. Helbig and others, that was published in a 2016 issue of the periodical.

Published
2017
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