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

✍ Scribed by Carlo Dionisi Vici; Alberto B. Burlina; Enrico Bertini; Claude Bachmann; Mercedes R.M. Mazziotta; F. Zacchello; Gaetano Sabetta; Daniel E. Hale

Book ID: 117161965
Publisher: Elsevier Science
Year: 1991
Tongue: English
Weight: 303 KB
Volume: 118
Category: Article
ISSN: 1097-6833
DOI: 10.1016/s0022-3476(05)80039-3

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