506 A specific form of ASD, known as Rett syndrome (clinically manifested with microcephaly, loss of motor coordination, stereotypic hand wringing, ataxia, seizures, and sleep disturbances) is caused by a loss of function mutation of the methyl-CpG-binding protein 2 or MECP2 gene, expressed in both neurones and neuroglia
AMP-Activated Protein Kinase in the Regulation of Hepatic Energy Metabolism: From Physiology to Therapeutic Perspectives
DePietro and Salzberg, 2022
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