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Genetics
CPT2 Deficiency
CPT2 deficiency for the FRACP written exam: the carnitine shuttle, the myopathic, infantile and neonatal phenotypes, triggers, the acylcarnitine profile and its limits between attacks, genetic diagnosis, acute and perioperative management, diet and carnitine, …
3 lessons and 0 exam-style questions, written for the RACP Divisional Written Exam
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