272 Inherited peripheral neuropathies: analysis of PDXK gene identifies a new treatable disorder

Viorica Chelban; Matthew Wilson; Natalia Zanetti; Eleni Zamba-Papanicolaou; Maria Conte; Carla Cordivari; Philippa Mills; Nicholas Wood; Peter Clayton; Henry Houlden

doi:10.1136/jnnp-2019-ABN-2.216

Article info

Parallel session 6: Clinical Neurology 2

272 Inherited peripheral neuropathies: analysis of PDXK gene identifies a new treatable disorder

Authors

Viorica Chelban Department of Neuromuscular Diseases, UCL Institute of Neurology PubMed articles Google scholar articles
Matthew Wilson Genetics and Genomic Medicine, GOS Institute of Child Health, UCL PubMed articles Google scholar articles
Natalia Zanetti Department of Clinical and Experimental Epilepsy, UCL Institute of Neurology PubMed articles Google scholar articles
Eleni Zamba-Papanicolaou The Cyprus Institute of Neurology and Genetics PubMed articles Google scholar articles
Maria Conte Randall Centre of Cell and Molecular Biophysics, School of Basic and Medical Biosciences, King’s College PubMed articles Google scholar articles
Carla Cordivari Clinical Neurophysiology Department National Hospital for Neurology and Neurosurgery PubMed articles Google scholar articles
Philippa Mills Genetics and Genomic Medicine, GOS Institute of Child Health, UCL PubMed articles Google scholar articles
Nicholas Wood Department of Neuromuscular Diseases, UCL Institute of Neurology PubMed articles Google scholar articles
Peter Clayton Genetics and Genomic Medicine, GOS Institute of Child Health, UCL PubMed articles Google scholar articles
Henry Houlden Department of Neuromuscular Diseases, UCL Institute of Neurology PubMed articles Google scholar articles

Citation

Chelban V, Wilson M, Zanetti N, et al

272 Inherited peripheral neuropathies: analysis of PDXK gene identifies a new treatable disorder

Journal of Neurology, Neurosurgery & Psychiatry 2019;90:e64.

Publication history

First published November 14, 2019.

Online issue publication

April 06, 2020

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