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Pyruvate dehydrogenase E1 alpha deficiency in a family: different clinical presentation in two siblings
L De Meirleir1, N Specola, S Seneca
1Pediatric Neurology and Medical Genetics, AZ-VUB Brussels, Belgium.
Journal of Inherited Metabolic Disease
|August 1, 1998
Abstract
No abstract available in PubMed .
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