Author:
Nobukuni Y.,Mitsubuchi H.,Ohta K.,Akaboshi I.,Indo Y.,Endo F.,Matsuda I.
Subject
Genetics(clinical),Genetics
Reference30 articles.
1. Danner DJ, Elsas II LJ (1989) Disorders of branched chain amino acid and keto acid metabolism. In Scriver CR, Beaudet AL, Sly WS, Valle D, eds.The Metabolic Basis of Inherited Disease, New York: McGraw-Hill, 671–692.
2. Danner DJ, Armstrong N, Heffelfinger SC, Sewell ET, Priest JH, Elsas LJ (1985) Absence of branched chain acyltransferase as a cause of maple syrup urine disease.J Clin Invest 75: 858–860.
3. Danner DJ, Litwer S, Herring WJ, Pruckler J (1989) Construction and nucleotide sequence of a cDNA encoding the full-length preprotein for human branched chain acyltransferase.J Biol Chem 264: 7742–7746.
4. Dancis J, Hutzler J, Snyderman SE (1972) Enzyme activity in classical and variant forms of maple syrup urine disease.J Pediatr 81: 312–320.
5. Dariush N, Fisher CW, Cox RP, Chuang DT (1991) Structure of the gene encoding the entire mature E1α subunit of human branched-chain α-keto acid dehydrogenase complex.FEBS Lett 284: 34–38.
Cited by
9 articles.
订阅此论文施引文献
订阅此论文施引文献，注册后可以免费订阅5篇论文的施引文献，订阅后可以查看论文全部施引文献