Associated Papers
Novel GNB4 Gene Variant and the Spectrum of GNB4 Variants in Patients With Charcot-Marie-Tooth Disease.
Pretkalnina D et al.
Neurology. Genetics, 2025
Clinical and Neuroimaging Features in Charcot-Marie-Tooth Patients with GNB4 Mutations.
Kwon HM et al.
Life (basel, Switzerland), 2021
The Emerging Role of Gβ Subunits in Human Genetic Diseases.
Malerba N et al.
Cells, 2019
Mutation spectrum of Charcot-Marie-Tooth disease among the Han Chinese in Taiwan.
Hsu YH et al.
Annals of Clinical and Translational Neurology, 2019
Letter regarding the article: "A novel missense variant (Gln220Arg) of GNB4 encoding guanine nucleotide-binding protein, subunit beta-4 in a Japanese family with autosomal dominant motor and sensory neuropathy".
Berciano J et al.
European Journal of Medical Genetics, 2018
A novel missense variant (Gln220Arg) of GNB4 encoding guanine nucleotide-binding protein, subunit beta-4 in a Japanese family with autosomal dominant motor and sensory neuropathy.
Miura S et al.
European Journal of Medical Genetics, 2017
Intermediate Charcot-Marie-Tooth disease: an electrophysiological reappraisal and systematic review.
Berciano J et al.
Journal of Neurology, 2017
Exome sequencing identifies GNB4 mutations as a cause of dominant intermediate Charcot-Marie-Tooth disease.
Soong BW et al.
American Journal of Human Genetics, 2013
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