Maternally inherited hypertrophic cardiomyopathy due to a novel T-to-C transition at nucleotide 9997 in the mitochondrial tRNA(glycine) gene.

Lignende værker

• Point mutation of the mitochondrial tRNA(Leu) gene (A 3243 G) in maternally inherited hypertrophic cardiomyopathy, diabetes mellitus, renal failure, and sensorineural deafness.
  af: Manouvrier, S, et al.
  Udgivet: (1995)
• Hypertrophic Cardiomyopathy due to Mitochondrial Disease: Prenatal Diagnosis, Management, and Outcome
  af: García-Díaz, Lutgardo, et al.
  Udgivet: (2013)
• Hypertrophic Cardiomyopathy due to Mitochondrial Disease: Prenatal Diagnosis, Management, and Outcome
  af: Lutgardo García-Díaz, et al.
  Udgivet: (2013-01-01)
• Maternally inherited cardiomyopathy and hearing loss associated with a novel mutation in the mitochondrial tRNA(Lys) gene (G8363A).
  af: Santorelli, F. M., et al.
  Udgivet: (1996)
• Co-inheritance of mutations associated with arrhythmogenic cardiomyopathy and hypertrophic cardiomyopathy
  af: De Bortoli, Marzia, et al.
  Udgivet: (2017)