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RT @FrontGenetics: New Research: Newborn Screening and Genetic Analysis Identify Six Novel Genetic Variants for Primary Carnitine Deficienc…
RT @FrontGenetics: New Research: Newborn Screening and Genetic Analysis Identify Six Novel Genetic Variants for Primary Carnitine Deficienc…
New Research: Newborn Screening and Genetic Analysis Identify Six Novel Genetic Variants for Primary Carnitine Deficiency in Ningbo Area, China: Primary carnitine deficiency (PCD) is an autosomal recessive disorder that could result in sudden… https://t.co