GDAP1 and Charcot-Marie-Tooth disease: An impairment in SOCE function related to a mislocalization of mitochondria close to Ca2+ entry sites has been shown to occur in Charcot-Marie-Tooth disease related to recessive mutations in ganglioside-induced differentiation associated protein 1 (GDAP1; Pla-Martín et al., 2013; González-Sánchez et al., 2017).