Analysis of theABCA4Gene by Next-Generation Sequencing
Investigative Ophthalmology & Visual Science2011Vol. 52(11), pp. 8479–8479
Citations Over TimeTop 10% of 2011 papers
Jana Zernant, Carl Schubert, Kate M. Im, Tomas R. Burke, Carolyn M. Brown, Gerald A. Fishman, Stephen H. Tsang, Peter Gouras, Michael Dean, Rando Allikmets
Abstract
Many mutations in the coding sequences of the ABCA4 gene are still unknown, and many possibly reside in noncoding regions of the ABCA4 locus. Although the ABCA4 array remains a good first-pass screening option, the NGS platform is a time- and cost-efficient tool for screening large cohorts.
Related Papers
- → Clinical and Genetic Spectrum of Stargardt Disease in Argentinean Patients(2021)13 cited
- → Genotype–Phenotype Association in ABCA4-Associated Retinopathy(2023)5 cited
- → Stargardt Disease Caused by a Rare Combination of Double Homozygous Mutations(2013)5 cited
- → Stargardt Disease(2014)1 cited
- Cosegregation analysis of mutant ABCA4 allleles in families with both Stargardt disease (STGD) and age–related macular degeneration (AMD).(2004)