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Almost all efficacy data come from a single research group, and independent replication of the larger-effect-size studies remains limited
It was designed and produced at the Institute of Molecular Genetics, Russian Academy of Sciences, in cooperation with the V.V
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Acylcarnitine profile Metabolites that are abnormal in VLCAD deficiency patients are usually C12, C14, C14:1, C14:2 and C16 [43], with C14:1 accumulation as most important marker, which is derived from partial breakdown of oleic acid (C18:1w9)
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