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Additionally, epigenetic regulation through DNA methylation and histone modifications may underlie increased long-term susceptibility to changes in bone and BMAT (193)
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Carnitine synthesis defect and autism With the overall goal to identify exonic copy number variants in the genome of ASD patients, Celestino-Soper and coauthors[42] analyzed 3743 samples for detecting disease-causing copy number variants (CNVs) that are not detected by most techniques used in conventional research and clinical diagnosis laboratories
