Disease: Charcot-Marie-Tooth disease- Type 2F
- A novel HSPB1 mutation associated with a late onset CMT2 phenotype: Case presentation and systematic review of the literature
- A novel HSPB1 mutation in an Italian patient with CMT2/dHMN phenotype
- A novel HSPB1<sup>S139F</sup> mouse model of Charcot-Marie-Tooth Disease
- A novel p.T139M mutation in HSPB1 highlighting the phenotypic spectrum in a family
- Bicyclic-Capped Histone Deacetylase 6 Inhibitors with Improved Activity in a Model of Axonal Charcot-Marie-Tooth Disease
- Characterization of New Transgenic Mouse Models for Two Charcot-Marie-Tooth-Causing HspB1 Mutations using the Rosa26 Locus
- Charcot Marie Tooth disease 2F and a novel mutation from India
- Charcot-Marie-Tooth 2F (Hsp27 mutations): A review
- Charcot-Marie-Tooth 2F: phenotypic presentation of the Arg136Leu HSP27 mutation in a multigenerational family
- Charcot-Marie-Tooth causing HSPB1 mutations increase Cdk5-mediated phosphorylation of neurofilaments
- Charcot-Marie-Tooth disease type 2F associated with biallelic HSPB1 mutations
- Clinical and genetic features of Charcot-Marie-Tooth disease 2F and hereditary motor neuropathy 2B in Japan
- Early and late manifestations of neuropathy due to HSPB1 mutation in the Jewish Iranian population
- Heterogeneous Clinical Phenotypes of dHMN Caused by Mutation in <em>HSPB1</em> Gene: A Case Series
- HSPB1 mutation causing distal Hereditary Motor Neuropathy type 2B in a Polish family
- HSPB1 mutations causing hereditary neuropathy in humans disrupt non-cell autonomous protection of motor neurons
- Mutant HSPB1 overexpression in neurons is sufficient to cause age-related motor neuronopathy in mice
- Mutations in heat shock protein beta-1 (HSPB1) are associated with a range of clinical phenotypes related to different patterns of motor neuron dysfunction: A case series
- Novel HDAC6 Inhibitors Increase Tubulin Acetylation and Rescue Axonal Transport of Mitochondria in a Model of Charcot-Marie-Tooth Type 2F
- Overexpression of mutant HSP27 causes axonal neuropathy in mice
- Small heat shock proteins operate as molecular chaperones in the mitochondrial intermembrane space