Leber’s hereditary optic neuropathy (LHON) in an Apulian cohort of subjects

Παρόμοια τεκμήρια

• Mitochondrial DNA copy number in affected and unaffected LHON mutation carriers
  ανά: Bianco, Angelica, κ.ά.
  Έκδοση: (2018)
• Leber’s hereditary optic neuropathy, intellectual disability and epilepsy presenting with variable penetrance associated to the m.3460G >A mutation and a heteroplasmic expansion of the microsatellite in MTRNR1 gene – case report
  ανά: Bianco, Angelica, κ.ά.
  Έκδοση: (2018)
• Increased Protein S-Glutathionylation in Leber’s Hereditary Optic Neuropathy (LHON)
  ανά: Zhou, Lei, κ.ά.
  Έκδοση: (2020)
• Pitfalls in the molecular genetic diagnosis of Leber hereditary optic neuropathy (LHON).
  ανά: Johns, D R, κ.ά.
  Έκδοση: (1993)
• Increased Protein <i>S</i>-Glutathionylation in Leber’s Hereditary Optic Neuropathy (LHON)
  ανά: Lei Zhou, κ.ά.
  Έκδοση: (2020-04-01)