SORDD: mutation frequency and phenotype in predominantly axonal Charcot-Marie-Tooth disease of undefined genetic cause

Annabelle Arlta Institute of Human Genetics, University of Münster, Münster, Germany;b Department of Neurology with Institute of Translational Neurology, University of Münster, Münster, GermanyView further author information

Esra Akova-Öztürkb Department of Neurology with Institute of Translational Neurology, University of Münster, Münster, GermanyView further author information

Anja Schirmacherc UKM Laboratory, University of Münster, Münster, GermanyView further author information

Bernhard Schlüterc UKM Laboratory, University of Münster, Münster, GermanyView further author information

Stephan Rustc UKM Laboratory, University of Münster, Münster, Germany;d Department of General Pediatrics, University of Münster, Münster, GermanyView further author information

Gerd Meyer zu Hörsteb Department of Neurology with Institute of Translational Neurology, University of Münster, Münster, GermanyView further author information

Heinz Wiendlb Department of Neurology with Institute of Translational Neurology, University of Münster, Münster, GermanyView further author information

Sarah Wiethoffb Department of Neurology with Institute of Translational Neurology, University of Münster, Münster, Germany;e UCL Queen Square Institute of Neurology, London, UKCorrespondence[email protected]
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SORDD: mutation frequency and phenotype in predominantly axonal Charcot-Marie-Tooth disease of undefined genetic cause

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SORDD: mutation frequency and phenotype in predominantly axonal Charcot-Marie-Tooth disease of undefined genetic cause

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