Published in Brain Dev on April 14, 2010
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Heterozygous UDP-GlcNAc 2-epimerase and N-acetylmannosamine kinase domain mutations in the GNE gene result in a less severe GNE myopathy phenotype compared to homozygous N-acetylmannosamine kinase domain mutations. J Neurol Sci (2012) 0.95
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Abnormal cerebral glucose metabolism in alternating hemiplegia of childhood. Brain Dev (2008) 0.88
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Decreased resting energy expenditure in patients with Duchenne muscular dystrophy. Brain Dev (2011) 0.88
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