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& Gutkind, J

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Compared to CM, fewer NRAS , BRAF mutations are seen in MM, but more SF3B1 mutation and KIT alterations are found

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Evaluation and Treatment of Patients with Autism and Mitochondrial Disease

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The study population for the analysis of recurrent CUD diagnosis in patients with T2D who had a prior diagnosis of CUD consisted of 8,196 patients

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Pritchard D

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