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Non-syndromic inherited retinal diseases in Poland: Genes, mutations, and phenotypes.
Tracewska, Anna M; Kocyla-Karczmarewicz, Beata; Rafalska, Agnieszka; Murawska, Joanna; Jakubaszko-Jablónska, Joanna; Rydzanicz, Malgorzata; Stawinski, Piotr; Ciara, Elzbieta; Lipska-Zietkiewicz, Beata S; Khan, Muhammad Imran; Cremers, Frans P M; Ploski, Rafal; Chrzanowska, Krystyna H.
Afiliación
  • Tracewska AM; Lukasiewicz Research Network - PORT Polish Center for Technology Development, Wroclaw, Poland.
  • Kocyla-Karczmarewicz B; Children's Memorial Health Institute, Warsaw, Poland.
  • Rafalska A; Department of Ophthalmology, Wroclaw Medical University, Wroclaw, Poland.
  • Murawska J; Department of Ophthalmology, University Clinical Centre, Gdansk, Poland.
  • Jakubaszko-Jablónska J; Department of Ophthalmology, Wroclaw Medical University, Wroclaw, Poland.
  • Rydzanicz M; Department of Paediatric Traumatology and Emergency Medicine, Wroclaw Medical University, Wroclaw, Poland.
  • Stawinski P; SPEKTRUM Ophthalmology Clinic, Wroclaw, Poland.
  • Ciara E; Department of Medical Genetics, Medical University of Warsaw, Warsaw, Poland.
  • Lipska-Zietkiewicz BS; Department of Medical Genetics, Medical University of Warsaw, Warsaw, Poland.
  • Khan MI; Children's Memorial Health Institute, Warsaw, Poland.
  • Cremers FPM; Centre for Rare Diseases, Medical University of Gdansk, Gdansk, Poland.
  • Ploski R; Department of Biology and Medical Genetics, Clinical Genetics Unit, Medical University of Gdansk, Gdansk, Poland.
  • Chrzanowska KH; Department of Human Genetics, Radboud University Medical Center, Nijmegen, The Netherlands.
Mol Vis ; 27: 457-465, 2021.
Article en En | MEDLINE | ID: mdl-34321860
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Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Enfermedades de la Retina / Enfermedades Hereditarias del Ojo / Genes / Mutación Tipo de estudio: Prevalence_studies / Risk_factors_studies Límite: Adolescent / Adult / Aged / Child / Child, preschool / Female / Humans / Infant / Male / Middle aged País/Región como asunto: Europa Idioma: En Revista: Mol Vis Asunto de la revista: BIOLOGIA MOLECULAR / OFTALMOLOGIA Año: 2021 Tipo del documento: Article País de afiliación: Polonia
Texto completo
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XML
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Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Enfermedades de la Retina / Enfermedades Hereditarias del Ojo / Genes / Mutación Tipo de estudio: Prevalence_studies / Risk_factors_studies Límite: Adolescent / Adult / Aged / Child / Child, preschool / Female / Humans / Infant / Male / Middle aged País/Región como asunto: Europa Idioma: En Revista: Mol Vis Asunto de la revista: BIOLOGIA MOLECULAR / OFTALMOLOGIA Año: 2021 Tipo del documento: Article País de afiliación: Polonia