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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.
Afiliação
  • 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 em En | MEDLINE | ID: mdl-32918965
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: DNA / DNA Mitocondrial / Atrofia Óptica Hereditária de Leber / Proteínas Mitocondriais / Metiltransferases / Mutação Tipo de estudo: Diagnostic_studies / Observational_studies Limite: Adult / Female / Humans Idioma: En Revista: Ophthalmology Ano de publicação: 2021 Tipo de documento: Article
Texto completo
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: DNA / DNA Mitocondrial / Atrofia Óptica Hereditária de Leber / Proteínas Mitocondriais / Metiltransferases / Mutação Tipo de estudo: Diagnostic_studies / Observational_studies Limite: Adult / Female / Humans Idioma: En Revista: Ophthalmology Ano de publicação: 2021 Tipo de documento: Article