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Postmortem analysis for two prevalent betaoxidation mutations in sudden infant death
In 1990, the disease loci in these patients with SMA were mapped to the same region in chromosome 5q13, and they were grouped into one clinical entity (5q-SMA, hereafter simply referred to as SMA) [5,6,7,8]
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Herein, we attempt to explain the role of carnitine in the pathogenesis of NAFLD, as shown in Figure 3
