Your browser doesn't support javascript.
loading
Nuclear DNA Mutation Causing a Phenotypic Leber Hereditary Optic Neuropathy Plus.
Mansukhani, Sasha A; Mehta, Dev G; Renaud, Deborah L; Whealy, Mark A; Chen, John J; Bhatti, M Tariq.
Affiliation
  • Mansukhani SA; Department of Ophthalmology, Mayo Clinic College of Medicine and Science, Rochester, Minnesota.
  • Mehta DG; Department of Neurology, Mayo Clinic College of Medicine and Science, Rochester, Minnesota.
  • Renaud DL; Department of Neurology, Mayo Clinic College of Medicine and Science, Rochester, Minnesota; Department of Pediatrics, Mayo Clinic College of Medicine and Science, Rochester, Minnesota.
  • Whealy MA; Department of Neurology, Mayo Clinic College of Medicine and Science, Rochester, Minnesota.
  • Chen JJ; Department of Ophthalmology, Mayo Clinic College of Medicine and Science, Rochester, Minnesota; Department of Neurology, Mayo Clinic College of Medicine and Science, Rochester, Minnesota.
  • Bhatti MT; Department of Ophthalmology, Mayo Clinic College of Medicine and Science, Rochester, Minnesota; Department of Neurology, Mayo Clinic College of Medicine and Science, Rochester, Minnesota. Electronic address: bhatti.muhammad@mayo.edu.
Ophthalmology ; 128(4): 628-631, 2021 04.
Article in En | MEDLINE | ID: mdl-32918965
Subject(s)
Key words
Fulltext
Add to My VHL
Print
XML
PubMed Links
Search on Google

Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: DNA / DNA, Mitochondrial / Optic Atrophy, Hereditary, Leber / Mitochondrial Proteins / Methyltransferases / Mutation Type of study: Diagnostic_studies / Observational_studies Limits: Adult / Female / Humans Language: En Journal: Ophthalmology Year: 2021 Document type: Article
Fulltext
Add to My VHL
Print
XML
PubMed Links
Search on Google

Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: DNA / DNA, Mitochondrial / Optic Atrophy, Hereditary, Leber / Mitochondrial Proteins / Methyltransferases / Mutation Type of study: Diagnostic_studies / Observational_studies Limits: Adult / Female / Humans Language: En Journal: Ophthalmology Year: 2021 Document type: Article