Corrigendum: Cinical, Metabolic, and Genetic Analysis and Follow-Up of Eight Patients With HIBCH Mutations Presenting With Leigh/Leigh-Like Syndrome

Samankaltaisia teoksia

• Cinical, Metabolic, and Genetic Analysis and Follow-Up of Eight Patients With HIBCH Mutations Presenting With Leigh/Leigh-Like Syndrome
  Tekijä: Wang, Junling, et al.
  Julkaistu: (2021)
• Clinical and biochemical characterization of 3-hydroxyisobutyryl-CoA hydrolase (HIBCH) deficiency that causes Leigh-like disease and ketoacidosis
  Tekijä: Yamada, Kenichiro, et al.
  Julkaistu: (2014)
• HIBCH mutations can cause Leigh-like disease with combined deficiency of multiple mitochondrial respiratory chain enzymes and pyruvate dehydrogenase
  Tekijä: Ferdinandusse, Sacha, et al.
  Julkaistu: (2013)
• Treatable Leigh-like encephalopathy presenting in adolescence
  Tekijä: Fassone, Elisa, et al.
  Julkaistu: (2013)
• Successful diagnosis of HIBCH deficiency from exome sequencing and positive retrospective analysis of newborn screening cards in two siblings presenting with Leigh’s disease
  Tekijä: Stiles, Ashlee R., et al.
  Julkaistu: (2015)