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Mitochondrial A3243G mutation results in corneal endothelial polymegathism.
Bakhoum, Mathieu F; Wu, Wei-Pu; White, Eugenia C; Sengillo, Jesse D; Sanfilippo, Christian; Morcos, Marcelle M; Freund, K Bailey; Perry, Henry D; Sarraf, David; Tsang, Stephen H.
Afiliação
  • Bakhoum MF; Jonas Children's Vision Care, and Bernard & Shirlee Brown Glaucoma Laboratory, Columbia University, New York, NY, USA.
  • Wu WP; Department of Ophthalmology, College of Physicians and Surgeons, Columbia University, New York, NY, USA.
  • White EC; Department of Ophthalmology, Nassau University Medical Center, East Meadow, NY, USA.
  • Sengillo JD; Jonas Children's Vision Care, and Bernard & Shirlee Brown Glaucoma Laboratory, Columbia University, New York, NY, USA.
  • Sanfilippo C; Department of Ophthalmology, College of Physicians and Surgeons, Columbia University, New York, NY, USA.
  • Morcos MM; Jonas Children's Vision Care, and Bernard & Shirlee Brown Glaucoma Laboratory, Columbia University, New York, NY, USA.
  • Freund KB; Jonas Children's Vision Care, and Bernard & Shirlee Brown Glaucoma Laboratory, Columbia University, New York, NY, USA.
  • Perry HD; Department of Ophthalmology, College of Physicians and Surgeons, Columbia University, New York, NY, USA.
  • Sarraf D; Stein Eye Institute, Department of Ophthalmology, David Geffen School of Medicine at UCLA, Los Angeles, CA, USA.
  • Tsang SH; Department of Ophthalmology, Nassau University Medical Center, East Meadow, NY, USA.
Graefes Arch Clin Exp Ophthalmol ; 256(3): 583-588, 2018 Mar.
Article em En | MEDLINE | ID: mdl-29376197
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Texto completo: 1 Base de dados: MEDLINE Assunto principal: DNA Mitocondrial / Mutação Puntual / Epitélio Corneano / Doenças Mitocondriais / Síndrome Endotelial Iridocorneana Tipo de estudo: Clinical_trials / Prognostic_studies Limite: Humans Idioma: En Revista: Graefes Arch Clin Exp Ophthalmol Ano de publicação: 2018 Tipo de documento: Article País de afiliação: Estados Unidos
Texto completo
Imprimir
XML
PubMed Links
Buscar no Google

Texto completo: 1 Base de dados: MEDLINE Assunto principal: DNA Mitocondrial / Mutação Puntual / Epitélio Corneano / Doenças Mitocondriais / Síndrome Endotelial Iridocorneana Tipo de estudo: Clinical_trials / Prognostic_studies Limite: Humans Idioma: En Revista: Graefes Arch Clin Exp Ophthalmol Ano de publicação: 2018 Tipo de documento: Article País de afiliação: Estados Unidos