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Association of Variants in TMEM45A With Keratoglobus.
Weiner, Chen; Hecht, Idan; Kotlyar, Alina; Shoshany, Nadav; Zadok, David; Elbaz, Uri; Segev, Fani; Maytal, Anat; Hachmo, Yafit; Michiels, Carine; De Backer, Olivier; Shomron, Noam; Einan-Lifshitz, Adi; Pras, Eran.
Afiliação
  • Weiner C; Matlow's Ophthalmo-genetic Laboratory, Department of Ophthalmology, Shamir Medical Center, Zerifin, Israel.
  • Hecht I; Sackler Faculty of Medicine, Tel Aviv University, Tel Aviv, Israel.
  • Kotlyar A; Sackler Faculty of Medicine, Tel Aviv University, Tel Aviv, Israel.
  • Shoshany N; Department of Ophthalmology, Shamir Medical Center, Zerifin, Israel.
  • Zadok D; Matlow's Ophthalmo-genetic Laboratory, Department of Ophthalmology, Shamir Medical Center, Zerifin, Israel.
  • Elbaz U; Matlow's Ophthalmo-genetic Laboratory, Department of Ophthalmology, Shamir Medical Center, Zerifin, Israel.
  • Segev F; Department of Ophthalmology, Shamir Medical Center, Zerifin, Israel.
  • Maytal A; Department of Ophthalmology, Shaare Zedek Medical Center Affiliated with the Hebrew University-Hadassah School of Medicine, Jerusalem, Israel.
  • Hachmo Y; Sackler Faculty of Medicine, Tel Aviv University, Tel Aviv, Israel.
  • Michiels C; Department of Ophthalmology, Rabin Medical Center, Schneider Hospital, Petah Tikva, Israel.
  • De Backer O; Sackler Faculty of Medicine, Tel Aviv University, Tel Aviv, Israel.
  • Shomron N; Goldschleger Eye Institute, Sheba Medical Center, Tel Hashomer, Israel.
  • Einan-Lifshitz A; Sackler Faculty of Medicine, Tel Aviv University, Tel Aviv, Israel.
  • Pras E; Department of Ophthalmology, Meir Medical Center, Kfar Saba, Israel.
JAMA Ophthalmol ; 139(10): 1089-1095, 2021 Oct 01.
Article em En | MEDLINE | ID: mdl-34410316
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Texto completo: 1 Base de dados: MEDLINE Assunto principal: Oftalmopatias Hereditárias / Ceratocone Idioma: En Ano de publicação: 2021 Tipo de documento: Article
Texto completo
Imprimir
XML
PubMed Links
Buscar no Google

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Oftalmopatias Hereditárias / Ceratocone Idioma: En Ano de publicação: 2021 Tipo de documento: Article