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Charcot-Marie-Tooth 2F (Hsp27 mutations): A review.
Schwartz NU. Schwartz NU. Neurobiol Dis. 2019 Oct;130:104505. doi: 10.1016/j.nbd.2019.104505. Epub 2019 Jun 15. Neurobiol Dis. 2019. PMID: 31212070 Review.
Charcot-Marie-Tooth disease is a commonly inherited form of neuropathy. Although named over 100 years ago, identification of subtypes of Charcot-Marie-Tooth has rapidly expanded in the preceding decades with the advancement of gene …
Charcot-Marie-Tooth disease is a commonly inherited form of neuropathy. Although named over 100 years ago, ident …
A novel HSPB1 mutation associated with a late onset CMT2 phenotype: Case presentation and systematic review of the literature.
Taga A, Cornblath DR. Taga A, et al. J Peripher Nerv Syst. 2020 Sep;25(3):223-229. doi: 10.1111/jns.12395. Epub 2020 Jul 8. J Peripher Nerv Syst. 2020. PMID: 32639100 Review.
Mutations in the HSPB1 gene are associated with Charcot-Marie-Tooth (CMT) disease type 2F (CMT2F) and distal hereditary motor neuropathy type 2 (dHMN2). ...
Mutations in the HSPB1 gene are associated with Charcot-Marie-Tooth (CMT) disease type 2F (CMT2F) …