Neuropathy due to bi-allelic SH3TC2 variants: genotype-phenotype correlation and natural history

Overview of attention for article published in Brain, March 2023

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RT @Brain1878: Rehbein et al. present findings from a longitudinal study of clinical phenotypes of adults and children with Charcot-Marie-T…

Rehbein et al. present findings from a longitudinal study of clinical phenotypes of adults and children with Charcot-Marie-Tooth disease type 4C caused by mutations in SH3TC2, including 14 previously unpublished variants. https://t.co/gEJmjf5yvY https:/…

Exploring the Natural History of #CharcotMarieTooth Disease Type 4C New in @Brain1878 from the Inherited #Neuropathy Consortium (INC): https://t.co/e9NbJumqze

Rehbein et al. present findings from a longitudinal study of the clinical phenotypes of adults and children with Charcot-Marie-Tooth disease type 4C caused by mutations in SH3TC2, including 14 previously unpublished variants. https://t.co/NO6yUVsxPk ht…

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