Neonatal diagnosis of long-chain 3-hydroxyacyl-CoA dehydrogenase deficiency and implications for newborn screening by tandem mass spectrometry

Authors
Carpenter, KH Wilcken, B
Citation
Kh. Carpenter et B. Wilcken, Neonatal diagnosis of long-chain 3-hydroxyacyl-CoA dehydrogenase deficiency and implications for newborn screening by tandem mass spectrometry, J INH MET D, 22(7), 1999, pp. 840-841
Citations number
3
Categorie Soggetti
Endocrinology, Nutrition & Metabolism
Journal title
JOURNAL OF INHERITED METABOLIC DISEASE
ISSN journal
01418955 → ACNP
Volume
22
Issue
7
Year of publication
1999
Pages
840 - 841
Database
ISI
SICI code
0141-8955(199910)22:7<840:NDOL3D>2.0.ZU;2-7