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Diagnostic genetic testing for patients with bilateral optic neuropathy and comparison of clinical features according to OPA1 mutation status.
Gaier, Eric D; Boudreault, Katherine; Nakata, Isao; Janessian, Maria; Skidd, Philip; DelBono, Elizabeth; Allen, Keri F; Pasquale, Louis R; Place, Emily; Cestari, Dean M; Stacy, Rebecca C; Rizzo, Joseph F; Wiggs, Janey L.
Afiliación
  • Gaier ED; Department of Ophthalmology, Harvard Medical School, Massachusetts Eye and Ear Infirmary Boston, MA.
  • Boudreault K; Department of Ophthalmology, Harvard Medical School, Massachusetts Eye and Ear Infirmary Boston, MA.
  • Nakata I; Department of Ophthalmology, Harvard Medical School, Massachusetts Eye and Ear Infirmary Boston, MA.
  • Janessian M; Department of Ophthalmology, Harvard Medical School, Massachusetts Eye and Ear Infirmary Boston, MA.
  • Skidd P; Departments of Ophthalmology and Neurology, University of Vermont College of Medicine, Burlington, MA.
  • DelBono E; Department of Ophthalmology, Harvard Medical School, Massachusetts Eye and Ear Infirmary Boston, MA.
  • Allen KF; Department of Ophthalmology, Harvard Medical School, Massachusetts Eye and Ear Infirmary Boston, MA.
  • Pasquale LR; Department of Ophthalmology, Harvard Medical School, Massachusetts Eye and Ear Infirmary Boston, MA.
  • Place E; Channing Division of Network Medicine, Brigham and Women's Hospital, Harvard Medical School, Boston, MA.
  • Cestari DM; Department of Ophthalmology, Harvard Medical School, Massachusetts Eye and Ear Infirmary Boston, MA.
  • Stacy RC; Department of Ophthalmology, Harvard Medical School, Massachusetts Eye and Ear Infirmary Boston, MA.
  • Rizzo JF; Department of Ophthalmology, Harvard Medical School, Massachusetts Eye and Ear Infirmary Boston, MA.
  • Wiggs JL; Department of Ophthalmology, Harvard Medical School, Massachusetts Eye and Ear Infirmary Boston, MA.
Mol Vis ; 23: 548-560, 2017.
Article en En | MEDLINE | ID: mdl-28848318
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Texto completo: 1 Colección: 01-internacional Banco de datos: MEDLINE Asunto principal: Enfermedades del Nervio Óptico / Pruebas Genéticas / GTP Fosfohidrolasas / Mutación Tipo de estudio: Diagnostic_studies / Prognostic_studies / Risk_factors_studies Límite: Adult / Female / Humans / Male / Middle aged Idioma: En Revista: Mol Vis Asunto de la revista: BIOLOGIA MOLECULAR / OFTALMOLOGIA Año: 2017 Tipo del documento: Article País de afiliación: Marruecos
Texto completo
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XML
PubMed Links
Buscar en Google

Texto completo: 1 Colección: 01-internacional Banco de datos: MEDLINE Asunto principal: Enfermedades del Nervio Óptico / Pruebas Genéticas / GTP Fosfohidrolasas / Mutación Tipo de estudio: Diagnostic_studies / Prognostic_studies / Risk_factors_studies Límite: Adult / Female / Humans / Male / Middle aged Idioma: En Revista: Mol Vis Asunto de la revista: BIOLOGIA MOLECULAR / OFTALMOLOGIA Año: 2017 Tipo del documento: Article País de afiliación: Marruecos