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Rett syndrome is caused by mutations in X-linked MECP2, encoding methyl-CpG-binding protein 2
Somatomedin-C/insulin-like growth factor-I and insulin-like growth factor-II mRNAs in rat fetal and adult tissues
as nutrient signals, to activate important pathways [mammalian target of rapamycin complex (mTORC) and autophagy]
The liver benefits require attention, particularly for patients with fatty liver disease
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