Author:
Tchan Michel,Westbrook M.,Wilcox G.,Cutler R.,Smith N.,Penman R.,Strauss B. J. G.,Wilcken B.
Publisher
Springer Berlin Heidelberg
Reference10 articles.
1. Di Cianni G, Miccoli R, Volpe L, Lencioni C, Del Prato S (2003) Intermediate metabolism in normal pregnancy and in gestational diabetes. Diabetes Metab Res Rev 19(4):259–270
2. Grunewald S, Hinrichs F, Wendel U (1998) Pregnancy in a woman with maple syrup urine disease. J Inherit Metab Dis 21(2):89–94
3. Herring WJ, Litwer S, Weber JL, Danner DJ (1991) Molecular genetic basis of maple syrup urine disease in a family with two defective alleles for branched chain acyltransferase and localization of the gene to human chromosome 1. Am J Hum Genet 48(2):342–350
4. Lee PJ (2006) Pregnancy issues in inherited metabolic disorders. J Inherit Metab Dis 29(2–3):311–316
5. Nobukuni Y, Mitsubuchi H, Akaboshi I et al (1991) Maple syrup urine disease. Complete defect of the E1 beta subunit of the branched chain alpha-ketoacid dehydrogenase complex due to a deletion of an 11-bp repeat sequence which encodes a mitochondrial targeting leader peptide in a family with the disease. J Clin Invest 87(5):1862–1866
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