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Absence of Genotype/Phenotype Correlations Requires Molecular Diagnostic to Ascertain Stargardt and Stargardt-Like Swiss Patients.
Buhler, Virginie M M; Berger, Lieselotte; Schaller, André; Zinkernagel, Martin S; Wolf, Sebastian; Escher, Pascal.
Affiliation
  • Buhler VMM; Department of Ophthalmology, Inselspital, Bern University Hospital, 3010 Bern, Switzerland.
  • Berger L; Department of BioMedical Research, University of Bern, 3010 Bern, Switzerland.
  • Schaller A; Department of Ophthalmology, Inselspital, Bern University Hospital, 3010 Bern, Switzerland.
  • Zinkernagel MS; Department of Human Genetics, Inselspital, Bern University Hospital, 3010 Bern, Switzerland.
  • Wolf S; Department of Ophthalmology, Inselspital, Bern University Hospital, 3010 Bern, Switzerland.
  • Escher P; Department of BioMedical Research, University of Bern, 3010 Bern, Switzerland.
Genes (Basel) ; 12(6)2021 05 26.
Article in En | MEDLINE | ID: mdl-34073554
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Full text: 1 Database: MEDLINE Main subject: Phenotype / Genetic Heterogeneity / Stargardt Disease Type of study: Diagnostic_studies / Prognostic_studies Country/Region as subject: Europa Language: En Journal: Genes (Basel) Year: 2021 Type: Article Affiliation country: Switzerland
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Full text: 1 Database: MEDLINE Main subject: Phenotype / Genetic Heterogeneity / Stargardt Disease Type of study: Diagnostic_studies / Prognostic_studies Country/Region as subject: Europa Language: En Journal: Genes (Basel) Year: 2021 Type: Article Affiliation country: Switzerland