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Journal: Int. J. Neonatal Screen., 2017
Volume: 3
Number: 10
Article:
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
Authors:
by
Leah Dowsett, Lauren Lulis, Can Ficicioglu and Sanmati Cuddapah
Link:
https://www.mdpi.com/2409-515X/3/2/10
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