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

Author： Dowsett Leah   Lulis Lauren   Ficicioglu Can   Cuddapah Sanmati  

Publisher： MDPI

E-ISSN： 2409-515x|3|2|10-10

ISSN： 2409-515x

Source： International Journal of Neonatal Screening, Vol.3, Iss.2, 2017-04, pp. : 10-10

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