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27. Consanguineous 3-methylcrotonyl-CoA carboxylase deficiency: early-onset necrotizing encephalopathy with lethal outcome. Baykal T; Gokcay GH; Ince Z; Dantas MF; Fowler B; Baumgartner MR; Demir F; Can G; Demirkol M J Inherit Metab Dis; 2005; 28(2):229-33. PubMed ID: 15877210 [TBL] [Abstract][Full Text] [Related]
28. Glycine and L-carnitine therapy in 3-methylcrotonyl-CoA carboxylase deficiency. Rutledge SL; Berry GT; Stanley CA; van Hove JL; Millington D J Inherit Metab Dis; 1995; 18(3):299-305. PubMed ID: 7474896 [TBL] [Abstract][Full Text] [Related]
29. Deficiency of propionyl-Co A carboxylase and methylcrotonyl-Co A carboxylase in a patient with methylcrotonylglycinuria. Weyler W; Sweetman L; Maggio DC; Nyhan WL Clin Chim Acta; 1977 May; 76(3):321-8. PubMed ID: 858206 [TBL] [Abstract][Full Text] [Related]
30. Isolated biotin-resistant 3-methylcrotonyl-CoA carboxylase deficiency in two sibs. Beemer FA; Bartlett K; Duran M; Ghneim HK; Wadman SK; Bruinvis L; Ketting D Eur J Pediatr; 1982 Jul; 138(4):351-4. PubMed ID: 7128647 [TBL] [Abstract][Full Text] [Related]
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