Primary carnitine deficiency (PCD) is a rare autosomal recessive disorder, caused by
deficiency in the plasma membrane carnitine transporter. In this report, we aimed to describe …

Screening and Diagnosis of Children with Primary Carnitine Deficiency in Zhejiang Province,
China | Health & Environmental Research Online (HERO) | US EPA Jump to main content US …

Primary carnitine deficiency (PCD) is a rare autosomal recessive disorder, caused by
deficiency in the plasma membrane carnitine transporter. In this report, we aimed to describe …

Primary carnitine deficiency (PCD) is a rare autosomal recessive disorder, caused by
deficiency in the plasma membrane carnitine transporter. In this report, we aimed to describe …

Primary carnitine deficiency (PCD) is a rare autosomal recessive disorder, caused by
deficiency in the plasma membrane carnitine transporter. In this report, we aimed to describe …