Acyl-CoA Dehydrogenase Deficiency and RS

A female infant with medium-chain acyl-CoA dehyrogenase (MCAD) deficiency who was diagnosed with Rett syndrome at 3.5 years is reported from Twenteborg Hospital, Almelo, and Wilhelmina Kinderziekenhuis, Utrecht, The Netherlands.

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Autor Principal: J Gordon Millichap (Author)
Formato: Libro
Publicado: Pediatric Neurology Briefs Publishers, 1994-05-01T00:00:00Z.
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3rd Floor Main Library

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Número de Clasificación: A1234.567
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