Clinical, biochemical, and molecular genetic characteristics of patients with primary carnitine deficiency identified by newborn screening in Shanghai, China

Overview of attention for article published in Frontiers in Genetics, December 2022

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New Research: Clinical, biochemical, and molecular genetic characteristics of patients with primary carnitine deficiency identified by newborn screening in Shanghai, China: Background: Primary carnitine deficiency (PCD) is an autosomal… https://t.co/VVVi6v

08 Dec 2022

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