Congenital Hyperinsulinism due to mutations in HNF4A and HADH
Author:
Publisher
Springer Science and Business Media LLC
Subject
Endocrinology,Endocrinology, Diabetes and Metabolism
Link
http://link.springer.com/content/pdf/10.1007/s11154-010-9148-y.pdf
Reference40 articles.
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3. He XY, Yang SY, Schulz H. Assay of L-3-hydroxyacyl-coenzyme A dehydrogenase with substrates of different chain lengths. Anal Biochem. 1989;180(1):105–9.
4. Vredendaal PJ, van den Berg I, Malingre HE, Stroobants AK, Olde Weghuis DE, Berger R. Human short-chain L-3-hydroxyacyl-CoA dehydrogenase: cloning and characterization of the coding sequence. Biochem Biophys Res Commun. 1996;223(3):718–23.
5. Vredendaal PJ, van den Berg I, Stroobants AK, van der AD, Malingre HE, Berger R. Structural organization of the human short-chain L-3-hydroxyacyl-CoA dehydrogenase gene. Mamm Genome. 1998;9(9):763–8.
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