Published in
MDPI, International Journal of Neonatal Screening, 2(3), p. 10, 2017
DOI: 10.3390/ijns3020010
Links
Tools
Utility of Genetic Testing for Confirmation of Abnormal Newborn Screening in Disorders of Long-Chain Fatty Acids: A Missed Case of Carnitine Palmitoyltransferase 1A (CPT1A) Deficiency
This paper is made freely available by the publisher.
Full text: Download
Data provided by 