Progressive neuropathy and recurrent myoglobinuria in a child with long-chain 3-hydroxyacyl-coenzyme A dehydrogenase deficiency.

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Published in J Pediatr on May 01, 1991

Authors

C Dionisi Vici1, A B Burlina, E Bertini, C Bachmann, M R Mazziotta, F Zacchello, G Sabetta, D E Hale

Author Affiliations

1: Department of Metabolism, Bambino Gesù Children's Hospital, Rome, Italy.

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