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Continue to ChatPrimary systemic carnitine deficiency: A Turkish case with a novel homozygous SLC22A5 mutation and 14 years follow-up - https://avesis.lokmanhekim.edu.tr/yayin/7fa4cd90-7800-462d-9edb-176fca54b1d8/primary-systemic-carnitine-deficiency-a-turkish-case-with-a-novel-homozygous-slc22a5-mutation-and-14-years-follow-up