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43. Compound heterozygosity in four asymptomatic siblings with medium-chain acyl-CoA dehydrogenase deficiency. Albers S; Levy HL; Irons M; Strauss AW; Marsden D J Inherit Metab Dis; 2001 Jun; 24(3):417-8. PubMed ID: 11486912 [No Abstract] [Full Text] [Related]
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49. Early diagnosis and treatment of neonatal medium-chain acyl-CoA dehydrogenase deficiency: report of two siblings. Catzeflis C; Bachmann C; Hale DE; Coates PM; Wiesmann U; Colombo JP; Joris F; Délèze G Eur J Pediatr; 1990 May; 149(8):577-81. PubMed ID: 2347356 [TBL] [Abstract][Full Text] [Related]
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55. New genetic defects in mitochondrial fatty acid oxidation and carnitine deficiency. Stanley CA Adv Pediatr; 1987; 34():59-88. PubMed ID: 3318304 [TBL] [Abstract][Full Text] [Related]
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