De novo KCNA2 mutations cause hereditary spastic paraplegia

Ann Neurol. 2017 Feb;81(2):326-328. doi: 10.1002/ana.24866.

Andreea Manole^{1

2}, Roope Männikkö^{1

2}, Michael G Hanna²; SYNAPS study group; Dimitri M Kullmann³, Henry Houlden^{1

2}

¹ Department of Molecular Neuroscience and Neurogenetics Laboratory, UCL Institute of Neurology, London, United Kingdom.
² MRC Centre for Neuromuscular Diseases, UCL Institute of Neurology, London, United Kingdom.
³ Department of Clinical and Experimental Epilepsy, UCL Institute of Neurology, London, United Kingdom.

No abstract available

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