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

פריטים דומים

• Cinical, Metabolic, and Genetic Analysis and Follow-Up of Eight Patients With HIBCH Mutations Presenting With Leigh/Leigh-Like Syndrome
  מאת: Wang, Junling, et al.
  יצא לאור: (2021)
• Clinical and biochemical characterization of 3-hydroxyisobutyryl-CoA hydrolase (HIBCH) deficiency that causes Leigh-like disease and ketoacidosis
  מאת: Yamada, Kenichiro, et al.
  יצא לאור: (2014)
• HIBCH mutations can cause Leigh-like disease with combined deficiency of multiple mitochondrial respiratory chain enzymes and pyruvate dehydrogenase
  מאת: Ferdinandusse, Sacha, et al.
  יצא לאור: (2013)
• Treatable Leigh-like encephalopathy presenting in adolescence
  מאת: Fassone, Elisa, et al.
  יצא לאור: (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
  מאת: Stiles, Ashlee R., et al.
  יצא לאור: (2015)