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

অনুরূপ উপাদানগুলি

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