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2020年2期

Journal of Translational Genetics and Genomics

上一期 下一期 浏览往期
Review
  • Redefining infantile-onset multisystem phenotypes of coenzyme Q10-deficiency in the next-generation sequencing era
  • Cryogenic electron paramagnetic resonance spectroscopy of flash-frozen tissue for characterization of mitochondrial disease
  • Role of transfer RNA modification and aminoacylation in the etiology of congenital intellectual disability
  • Mitochondrial translation defects and human disease
Original Article
  • The North American mitochondrial disease registry
  • Spectrum of MECP2 mutations in Indian females with Rett Syndrome - a large cohort study
Opinion
  • Intellectual disability, the long way from genes to biological mechanisms

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