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Mutations in the GTPases optic atrophy 1 (OPA1) and Mfn2 are associated with autosomal dominant optic atrophy and Charcot-Marie-Tooth neuropathy type 2A, and suggest a role for abnormal mitochondrial fusion in the pathogenesis of these human diseases (Larrea et al., 2019)

The thin needles minimize tissue damage during injections

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This delayed gastric emptying contributes to feelings of fullness and helps in controlling post-prandial blood sugar levels