Mitochondrial dysfunction, metabolic quiescence and premature senescence in CMT4B3 fibroblasts
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Charcot-Marie-Tooth disease type 4B3 (CMT4B3) is an ultra-rare autosomal recessive neuropathy caused by mutations in the MTMR5/SBF1 gene. In this study, we characterized dermal fibroblasts derived from a patient carrying compound-heterozygous MTMR5/SBF1 varian... ...
