Disorders of carnitine transport and the carnitine cycle
Author:
Publisher
Wiley
Subject
Genetics (clinical),Genetics
Reference41 articles.
1. Detection of Neonatal Carnitine Palmitoyltransferase II Deficiency by Expanded Newborn Screening With Tandem Mass Spectrometry
2. Tyrosine Residues Affecting Sodium Stimulation of Carnitine Transport in the OCTN2 Carnitine/Organic Cation Transporter
3. Novel mutations in CPT 1A define molecular heterogeneity of hepatic carnitine palmitoyltransferase I deficiency
4. CARNITINE
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