Motor neuron diseases caused by a novel VRK1 variant – A genotype/phenotype study

Motor neuron diseases caused by a novel VRK1 variant – A genotype/phenotype study

Abstract Background Motor neuron disorders involving upper and lower neurons are a genetically and clinically heterogenous group of rare neuromuscular disorders with overlap among spinal muscular atrophies (SMAs) and amyotrophic lateral sclerosis (ALS). Classical SMA caused by recessive mutations in...

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Bibliographic Details
Main Authors: Maryam Sedghi, Ali‐Reza Moslemi, Montse Olive, Masoud Etemadifar, Behnaz Ansari, Jafar Nasiri, Leila Emrahi, Hamid‐Reza Mianesaz, Nigel G. Laing, Homa Tajsharghi
Format: Article
Language:English
Published: Wiley 2019-11-01
Series:Annals of Clinical and Translational Neurology
Online Access:https://doi.org/10.1002/acn3.50912

Internet

https://doi.org/10.1002/acn3.50912

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