Spectrum of movement disorders and neurotransmitter abnormalities in paediatric POLG disease

Antzeko izenburuak

• Depletion of mitochondrial DNA in fibroblast cultures from patients with POLG1 mutations is a consequence of catalytic mutations.
  nork: Ashley, N, et al.
  Argitaratua: (2008)
• Depletion of mitochondrial DNA in fibroglast cultures from patients with POLG1 mutations is a consequence of catalytic mutations
  nork: Ashley, N, et al.
  Argitaratua: (2008)
• Collated mutations in mitochondrial DNA (mtDNA) depletion syndrome (excluding the mitochondrial gamma polymerase, POLG1).
  nork: Poulton, J, et al.
  Argitaratua: (2009)
• POLG Novel Mutation with Alpers Syndrome
  nork: J Gordon Millichap
  Argitaratua: (2012-02-01)
• Zebrafish polg2 knock-out recapitulates human POLG-disorders; implications for drug treatment
  nork: Raquel Brañas Casas, et al.
  Argitaratua: (2024-04-01)