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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

S.TanabeN.AhangariF.VerledenS

doi: 10.1021/acschembio.5b00900 55 SchilstraMJVeldinkGAVliegenthartJF

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This immune activation likely contributes to both pain and the fatigue and cognitive symptoms characteristic of the condition

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