• <em>MPV17-</em>Related Mitochondrial DNA Maintenance Defect
• <em>MPV17</em>-related Hepatocerebral Mitochondrial DNA Depletion Syndrome
• A Drosophila model of the neurological symptoms in Mpv17-related diseases
• A novel homozygous MPV17 mutation in two families with axonal sensorimotor polyneuropathy
• A Yeast-Based Repurposing Approach for the Treatment of Mitochondrial DNA Depletion Syndromes Led to the Identification of Molecules Able to Modulate the dNTP Pool
• Hand involvement in Navajo neurohepatopathy: a case report
• Hepatocellular neoplasms arising in genetic metabolic disorders: steatosis is common in both the tumor and background liver
• MPV17 mutations in juvenile- and adult-onset axonal sensorimotor polyneuropathy
• MPV17 mutations in patients with hepatocerebral mitochondrial DNA depletion syndrome
• MPV17-related hepatocerebral mitochondrial DNA depletion syndrome (MPV17-NNH) revisited
• MPV17-related mitochondrial DNA maintenance defect: New cases and review of clinical, biochemical, and molecular aspects
• Navajo Neurohepatopathy : A Case Report and Literature Review Emphasizing Clinicopathologic Diagnosis
• Outcomes after liver transplantation in MPV17 deficiency (Navajo neurohepatopathy): A single-center case series
• Outcomes after liver transplantation in MPV17 deficiency: A rebuttal
• The long-term outcomes after liver transplantation in MPV-17 deficiency (Navajo Neurohepatopathy) are poor