Mitochondrial cardioencephalopathy due to a COQ4 mutation

Lignende værker

• Fibroblast growth-factor-21 is currently a weak biomarker for identifying mitochondrial and non-mitochondrial inborn errors of metabolism
  af: Josef Finsterer, et al.
  Udgivet: (2018-03-01)
• Kearns-Sayre syndrome is genetically and phenotypically heterogeneous
  af: Josef Finsterer, et al.
  Udgivet: (2018-05-01)
• Mitochondrial myopathy, dysmorphism, exercise-induced vomiting and tachycardia the mutation m.4831G > A
  af: Josef Finsterer, et al.
  Udgivet: (2017-06-01)
• Phenotypic heterogeneity of a compound heterozygous SUCLA2 mutation
  af: Josef Finsterer, et al.
  Udgivet: (2017-03-01)
• KEARNS-SAYRE SYNDROME MIGHT BE MIXED UP WITH CPEO PLUS
  af: Josef Finsterer, et al.
  Udgivet: (2019-01-01)