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2. 3-methylcrotonyl-CoA carboxylase deficiency in an infant with cardiomyopathy, in her brother with developmental delay and in their asymptomatic father. Visser G; Suormala T; Smit GP; Reijngoud DJ; Bink-Boelkens MT; Niezen-Koning KE; Baumgartner ER Eur J Pediatr; 2000 Dec; 159(12):901-4. PubMed ID: 11131348 [TBL] [Abstract][Full Text] [Related]
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