3-Methylglutaconic aciduria: Familial neonatal form with fatal onset
Author:
Publisher
Wiley
Subject
Genetics(clinical),Genetics
Link
http://www.springerlink.com/index/pdf/10.1007/BF01811428
Reference10 articles.
1. Duran, M., Beemer, F. A., Tibosch, A. S., Bruinvis, A. S., Ketting, D. and Wadman, S. K. Inherited 3-methylglutaconic aciduria in two brothers. Another defect of leucine metabolism.J. Pediatr. 101 (1982) 551–554
2. Edmond, J. and Popjak, G. Transfer of carbon atoms from mevalonate to n-fatty acids.J. Biol. Chem. 10 (1974) 66–71
3. Gibson, K. M., Sweetman, L., Nyhan, W. L., Narisawa, K., Roth, K., Lehnert, W., Robinson, B., Duran, M. and Wadman, S. K. 3-Methylglutaconyl-CoA hydratase deficiency: two different clinical and enzymatic phenotypes in 3-methylglutaconic aciduria.Pediatr. Res. 19 (1985) 248a
4. Greter, J., Hagberg, B., Steen G. and Söderhjelm, U. 3-Methylglutaconic aciduria: report on a sibship with infantile progressive encephalopathy.Eur. J. Pediatr. 129 (1978) 231–238
5. Hagberg, B., Hjalmarson, O., Lindstedt, S., Ransnäs, L. and Steen, G. 3-Methylglutaconic aciduria in two infants.Clin. Chim. Acta 134 (1983) 59–67
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