Correspondence to: “Heterozygous mutation in the X chromosomal NDUFA1 gene in a girl with complex I deficiency” and “A novel NDUFA1 mutation leads to progressive mitochondrial complex I- specific neurodegenerative disease”

Registos relacionados

• A novel NDUFA1 mutation leads to a progressive mitochondrial complex I- specific neurodegenerative disease
  Por: Potluri, Prasanth, et al.
  Publicado em: (2009)
• NDUFA2 Complex I Mutation Leads to Leigh Disease
  Por: Hoefs, Saskia J.G., et al.
  Publicado em: (2008)
• NDUFA10 mutations cause complex I deficiency in a patient with Leigh disease
  Por: Hoefs, Saskia J G, et al.
  Publicado em: (2011)
• Compound Heterozygous Mutation of Rag1 Leading to Omenn Syndrome
  Por: Matthews, Adam G. W., et al.
  Publicado em: (2015)
• The NDUFA1 gene product (MWFE protein) is essential for activity of complex I in mammalian mitochondria
  Por: Au, Harry C., et al.
  Publicado em: (1999)