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While exploration of DNA methylation patterns in children with acute undernutrition and obesity has garnered significant attention, research on other layers of epigenetic regulation, such as histone modifications and microRNAs, remains scarce

PMCID: PMC3580441

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[3] In humans, defects in GSS are inherited in an autosomal recessive way and are the cause of severe metabolic acidosis, 5-oxoprolinuria, increased rate of haemolysis, and defective function of the central nervous system

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