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Genetics and Disease Expression in the CNGA3 Form of Achromatopsia: Steps on the Path to Gene Therapy.
Zelinger, Lina; Cideciyan, Artur V; Kohl, Susanne; Schwartz, Sharon B; Rosenmann, Ada; Eli, Dalia; Sumaroka, Alexander; Roman, Alejandro J; Luo, Xunda; Brown, Cassondra; Rosin, Boris; Blumenfeld, Anat; Wissinger, Bernd; Jacobson, Samuel G; Banin, Eyal; Sharon, Dror.
Afiliação
  • Zelinger L; Department of Ophthalmology, Hadassah Hebrew University Medical Center, Jerusalem, Israel.
  • Cideciyan AV; Department of Ophthalmology, Scheie Eye Institute, University of Pennsylvania, Philadelphia, Pennsylvania.
  • Kohl S; Molecular Genetics Laboratory, Institute for Ophthalmic Research, Centre for Ophthalmology, University of Tübingen, Tübingen, Germany.
  • Schwartz SB; Department of Ophthalmology, Scheie Eye Institute, University of Pennsylvania, Philadelphia, Pennsylvania.
  • Rosenmann A; Department of Ophthalmology, Hadassah Hebrew University Medical Center, Jerusalem, Israel.
  • Eli D; Department of Ophthalmology, Hadassah Hebrew University Medical Center, Jerusalem, Israel.
  • Sumaroka A; Department of Ophthalmology, Scheie Eye Institute, University of Pennsylvania, Philadelphia, Pennsylvania.
  • Roman AJ; Department of Ophthalmology, Scheie Eye Institute, University of Pennsylvania, Philadelphia, Pennsylvania.
  • Luo X; Department of Ophthalmology, Scheie Eye Institute, University of Pennsylvania, Philadelphia, Pennsylvania.
  • Brown C; Department of Ophthalmology, Scheie Eye Institute, University of Pennsylvania, Philadelphia, Pennsylvania.
  • Rosin B; Department of Ophthalmology, Hadassah Hebrew University Medical Center, Jerusalem, Israel.
  • Blumenfeld A; Department of Ophthalmology, Hadassah Hebrew University Medical Center, Jerusalem, Israel.
  • Wissinger B; Molecular Genetics Laboratory, Institute for Ophthalmic Research, Centre for Ophthalmology, University of Tübingen, Tübingen, Germany.
  • Jacobson SG; Department of Ophthalmology, Scheie Eye Institute, University of Pennsylvania, Philadelphia, Pennsylvania.
  • Banin E; Department of Ophthalmology, Hadassah Hebrew University Medical Center, Jerusalem, Israel.
  • Sharon D; Department of Ophthalmology, Hadassah Hebrew University Medical Center, Jerusalem, Israel. Electronic address: dror.sharon1@gmail.com.
Ophthalmology ; 122(5): 997-1007, 2015 May.
Article em En | MEDLINE | ID: mdl-25616768
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Degeneração Retiniana / Terapia Genética / Defeitos da Visão Cromática / Efeito Fundador / Canais de Cátion Regulados por Nucleotídeos Cíclicos / Mutação Tipo de estudo: Guideline / Risk_factors_studies Limite: Adolescent / Adult / Child / Female / Humans / Male / Middle aged País/Região como assunto: Asia Idioma: En Revista: Ophthalmology Ano de publicação: 2015 Tipo de documento: Article País de afiliação: Israel País de publicação: Estados Unidos
Texto completo
Adicionar na Minha BVS
Imprimir
XML
PubMed Links
Buscar no Google

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Degeneração Retiniana / Terapia Genética / Defeitos da Visão Cromática / Efeito Fundador / Canais de Cátion Regulados por Nucleotídeos Cíclicos / Mutação Tipo de estudo: Guideline / Risk_factors_studies Limite: Adolescent / Adult / Child / Female / Humans / Male / Middle aged País/Região como assunto: Asia Idioma: En Revista: Ophthalmology Ano de publicação: 2015 Tipo de documento: Article País de afiliação: Israel País de publicação: Estados Unidos