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FOXC1 variant in a family with anterior segment dysgenesis and normal-tension glaucoma.
Or, Lior; Barkana, Yaniv; Hecht, Idan; Weiner, Chen; Einan-Lifshitz, Adi; Pras, Eran.
Afiliação
  • Or L; Department of Ophthalmology, Shamir Medical Center, Israel; Sackler Faculty of Medicine, Tel Aviv University, Tel Aviv, Israel. Electronic address: orlior555@gmail.com.
  • Barkana Y; Private Practice, Ramla, Israel.
  • Hecht I; Department of Ophthalmology, Shamir Medical Center, Israel; Sackler Faculty of Medicine, Tel Aviv University, Tel Aviv, Israel.
  • Weiner C; Sackler Faculty of Medicine, Tel Aviv University, Tel Aviv, Israel; Matlow's Ophthalmo-genetic Laboratory, Department of Ophthalmology, Shamir Medical Center, Israel.
  • Einan-Lifshitz A; Department of Ophthalmology, Shamir Medical Center, Israel; Sackler Faculty of Medicine, Tel Aviv University, Tel Aviv, Israel.
  • Pras E; Department of Ophthalmology, Shamir Medical Center, Israel; Sackler Faculty of Medicine, Tel Aviv University, Tel Aviv, Israel; Matlow's Ophthalmo-genetic Laboratory, Department of Ophthalmology, Shamir Medical Center, Israel.
Exp Eye Res ; 200: 108220, 2020 11.
Article em En | MEDLINE | ID: mdl-32905845
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Texto completo: 1 Base de dados: MEDLINE Assunto principal: DNA / Anormalidades do Olho / Fatores de Transcrição Forkhead / Glaucoma de Baixa Tensão / Mutação Idioma: En Ano de publicação: 2020 Tipo de documento: Article
Texto completo
Imprimir
XML
PubMed Links
Buscar no Google

Texto completo: 1 Base de dados: MEDLINE Assunto principal: DNA / Anormalidades do Olho / Fatores de Transcrição Forkhead / Glaucoma de Baixa Tensão / Mutação Idioma: En Ano de publicação: 2020 Tipo de documento: Article