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Description
Rett syndrome (RS) is caused by mutations in the gene methyl-CpG-binding protein 2 (MECP2) Rett syndrome RS is characterized by language and communication problems, learning and coordination difficulties, and they display autistic-like behaviors [362, 363]
as well as various other nonillustrated results lay out converging evidence of sex-specific metabolic patterns
Internal body biomarkers are being studied to look for changes in the body that can prevent the onset of additional health issues
funding acquisition, A.C.-G
