Identification of rare variants in the FBXO38 gene of patients with chronic inflammatory demyelinating polyradiculoneuropathy
Author:
Funder
Hospices Civils de Lyon
Publisher
Elsevier BV
Reference18 articles.
1. A novel homozygous FBXO38 variant causes an early-onset distal hereditary motor neuronopathy type IID;Akçimen;J. Hum. Genet.,2019
2. Genetics of Guillain-Barré syndrome (GBS) and chronic inflammatory demyelinating polyradiculoneuropathy (CIDP): current knowledge and future directions;Blum;J. Peripheral. Nervous. Sys.,2014
3. Progress in diagnosis and treatment of chronic inflammatory demyelinating polyradiculoneuropathy;Bunschoten;Lancet Neurol.,2019
4. Variations of the perforin gene in patients with chronic inflammatory demyelinating polyradiculoneuropathy;Buttini;Genes Immun.,2015
5. Cerebellar involvement associated with immune checkpoint inhibitors: a systematic review;Dinoto;Eur. J. Neurol.,2023
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