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Mitochondria are dynamic organelles that continually move, fuse and divide. The dynamic balance of fusion and fission of… Expand ABSTRACT Alcohol dependence is a severe disorder contributing substantially to the global burden of disease. Despite the… Expand Charcot‐Marie‐Tooth disease type 4C (CMT4C) is an autosomal recessive (AR) demyelinating neuropathy associated to SH3TC2… Expand Objective: To investigate whether mutations in the SURF1 gene are a cause of Charcot-Marie-Tooth (CMT) disease. Methods: We… Expand The prevalence of Charcot‐Marie‐Tooth (CMT) disease or hereditary motor and sensory neuropathy (HMSN) varies in different… Expand Autosomal recessive Charcot-Marie-Tooth diseases, relatively common in Algeria due to high prevalence of consanguineous marriages… Expand Charcot-Marie-Tooth (CMT) disease is a category of hereditary neuropathy. Rather than 1 disease, CMT is a syndrome of several… Expand Autosomal recessive demyelinating Charcot-Marie-Tooth disease (CMT4), Dejerine-Sottas disease and congenital hypomyelinating… Expand By data mining in the sequence of the Corynebacterium glutamicum ATCC 13032 genome, six putative mycolyltransferase genes were… Expand Autosomal recessive Charcot-Marie-Tooth (CMT) disease (CMT4) is a complex group of severe childhood motor and sensory… Expand