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Common and rare variants in patients with early onset drusen maculopathy.
de Breuk, Anita; Lechanteur, Yara T E; Astuti, Galuh; Galbany, Jordi Corominas; Klaver, Caroline C W; Hoyng, Carel B; den Hollander, Anneke I.
Afiliação
  • de Breuk A; Department of Ophthalmology, Donders Institute for Brain, Cognition and Behaviour, Radboud University Medical Center, Nijmegen, The Netherlands.
  • Lechanteur YTE; Department of Ophthalmology, Donders Institute for Brain, Cognition and Behaviour, Radboud University Medical Center, Nijmegen, The Netherlands.
  • Astuti G; Department of Human Genetics, Radboud University Medical Center, Nijmegen, The Netherlands.
  • Galbany JC; Division of Human Genetics, Center for Biomedical Research, Faculty of Medicine, Diponegoro University, Semarang, Indonesia.
  • Klaver CCW; Department of Human Genetics, Radboud University Medical Center, Nijmegen, The Netherlands.
  • Hoyng CB; Department of Ophthalmology, Donders Institute for Brain, Cognition and Behaviour, Radboud University Medical Center, Nijmegen, The Netherlands.
  • den Hollander AI; Department of Ophthalmology, Department of Epidemiology, Erasmus Medical Center, Rotterdam, The Netherlands.
Clin Genet ; 102(5): 414-423, 2022 11.
Article em En | MEDLINE | ID: mdl-36053979
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Fator H do Complemento / Degeneração Macular Tipo de estudo: Prognostic_studies Aspecto: Patient_preference Limite: Humans Idioma: En Revista: Clin Genet Ano de publicação: 2022 Tipo de documento: Article
Texto completo
Imprimir
XML
PubMed Links
Buscar no Google

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Fator H do Complemento / Degeneração Macular Tipo de estudo: Prognostic_studies Aspecto: Patient_preference Limite: Humans Idioma: En Revista: Clin Genet Ano de publicação: 2022 Tipo de documento: Article