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High-Throughput Sequencing to Identify Mutations Associated with Retinal Dystrophies.
Song, Fei; Owczarek-Lipska, Marta; Ahmels, Tim; Book, Marius; Aisenbrey, Sabine; Menghini, Moreno; Barthelmes, Daniel; Schrader, Stefan; Spital, Georg; Neidhardt, John.
Afiliação
  • Song F; Human Genetics Faculty VI-School of Medicine and Health Sciences, University of Oldenburg, Ammerländer Heerstrasse 114-118, 26129 Oldenburg, Germany.
  • Owczarek-Lipska M; Human Genetics Faculty VI-School of Medicine and Health Sciences, University of Oldenburg, Ammerländer Heerstrasse 114-118, 26129 Oldenburg, Germany.
  • Ahmels T; Research Center Neurosensory Science, University of Oldenburg, 26129 Oldenburg, Germany.
  • Book M; Department of Ophthalmology, Pius-Hospital, University of Oldenburg, 26121 Oldenburg, Germany.
  • Aisenbrey S; Eye Centre at the St. Franziskus Hospital, 48145 Münster, Germany.
  • Menghini M; Department of Ophthalmology, Vivantes Health Network Ltd., Neukölln Hospital, 12351 Berlin, Germany.
  • Barthelmes D; Department of Ophthalmology, Ospedale Regionale di Lugano, 6900 Lugano, Switzerland.
  • Schrader S; Department of Ophthalmology, University Hospital Zurich, University of Zurich, 8091 Zurich, Switzerland.
  • Spital G; Department of Ophthalmology, University Hospital Zurich, University of Zurich, 8091 Zurich, Switzerland.
  • Neidhardt J; Department of Ophthalmology, Pius-Hospital, University of Oldenburg, 26121 Oldenburg, Germany.
Genes (Basel) ; 12(8)2021 08 20.
Article em En | MEDLINE | ID: mdl-34440443
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Transportadores de Cassetes de Ligação de ATP / Predisposição Genética para Doença / Distrofias Retinianas / Aconselhamento Genético Tipo de estudo: Diagnostic_studies / Prognostic_studies / Risk_factors_studies Limite: Female / Humans / Male / Middle aged Idioma: En Revista: Genes (Basel) Ano de publicação: 2021 Tipo de documento: Article País de afiliação: Alemanha
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: Transportadores de Cassetes de Ligação de ATP / Predisposição Genética para Doença / Distrofias Retinianas / Aconselhamento Genético Tipo de estudo: Diagnostic_studies / Prognostic_studies / Risk_factors_studies Limite: Female / Humans / Male / Middle aged Idioma: En Revista: Genes (Basel) Ano de publicação: 2021 Tipo de documento: Article País de afiliação: Alemanha