Glycogen-Storage Disease Type II
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Clinical Approach to Inherited Peroxisomal Disorders: A Series of 27 Patients
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Canavan Disease:From Spongy Degeneration to Molecular Analysis
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Chronic Cardiomyopathy and WEakness or Acute Coma in Children with a Defect in Carnitine Uptake
Ann Neurol 30:709-716, Stanley,C.A.,et al, 1991
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