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19. Rett syndrome in a patient with medium chain acyl-CoA dehydrogenase deficiency. Beekman RP; Hofstee N; Smeitink JA; Poll-The BT; Duran M Eur J Pediatr; 1994 Apr; 153(4):264-6. PubMed ID: 8194560 [TBL] [Abstract][Full Text] [Related]
20. Screening of the most common medium-chain acyl CoA dehydrogenase (MCAD) deficiency mutation (K329E) in the Czech newborn population. Kozàk L; Hrabincovà E; Rudolfoà J; Vràbelovà S; Freiberger T Southeast Asian J Trop Med Public Health; 1999; 30 Suppl 2():49-50. PubMed ID: 11400780 [TBL] [Abstract][Full Text] [Related] [Next] [New Search]