The genetic basis of isolated mitochondrial complex II deficiency

Lignende værker

• Recessive germline SDHA and SDHB mutations causing leukodystrophy and isolated mitochondrial complex II deficiency
  af: Alston, Charlotte L, et al.
  Udgivet: (2012)
• Recent advances in understanding the molecular genetic basis of mitochondrial disease
  af: Thompson, Kyle, et al.
  Udgivet: (2019)
• Using a quantitative quadruple immunofluorescent assay to diagnose isolated mitochondrial Complex I deficiency
  af: Ahmed, Syeda T., et al.
  Udgivet: (2017)
• Use of whole exome sequencing to determine the genetic basis of multiple mitochondrial respiratory chain complex deficiency
  af: Taylor, Robert W., et al.
  Udgivet: (2014)
• A recessive homozygous p.Asp92Gly SDHD mutation causes prenatal cardiomyopathy and a severe mitochondrial complex II deficiency
  af: Alston, Charlotte L., et al.
  Udgivet: (2015)