Richiedi una copia del documento: Dysregulation of the TRK-Fused Gene (TFG)/ULK1/LC3 axis in Hereditary Motor and Sensory Neuropathy with Proximal dominant involvement (HMSN-P), recessive hereditary Spastic Paraplegia (SPG 57), and Charcot-Marie-Tooth disease 2 (CMT2)

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