A Comprehensive Survey of Sequence Variation in the ABCA4 (ABCR) Gene in Stargardt Disease and Age-Related Macular Degeneration
The American Journal of Human Genetics2000Vol. 67(4), pp. 800–813
Citations Over TimeTop 10% of 2000 papers
Andrea Rivera, Karen L. White, Heidi Stöhr, Klaus Steiner, Nadine Hemmrich, T. Grimm, Bernhard Jurklies, Birgit Lorenz, Hendrik P. N. Scholl, E Apfelstedt-Sylla, Bernhard H. F. Weber
Related Papers
- → Clinical and Genetic Spectrum of Stargardt Disease in Argentinean Patients(2021)13 cited
- → Stargardt Disease Caused by a Rare Combination of Double Homozygous Mutations(2013)5 cited
- → CRISPR-Cas9 in hiPSCs: A new era in personalized treatment for Stargardt disease(2023)3 cited
- → Stargardt Disease(2014)1 cited
- → ABCA4- Related Retinopathies in Lebanon: a novel mutation and significant heterogeneity(2023)