Long-read technologies identify a hidden inverted duplication in a family with choroideremia

The lack of molecular diagnoses in rare genetic diseases can be explained by limitations of current standard genomic technologies. Upcoming long-read techniques have complementary strengths to overcome these limitations, with a particular strength in identifying structural variants. By using optical...

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Detalles Bibliográficos
Autores principales: Fadaie, Zeinab, Neveling, Kornelia, Mantere, Tuomo, Derks, Ronny, Haer-Wigman, Lonneke, den Ouden, Amber, Kwint, Michael, O’Gorman, Luke, Valkenburg, Dyon, Hoyng, Carel B., Gilissen, Christian, Vissers, Lisenka E.L.M., Nelen, Marcel, Cremers, Frans P.M., Hoischen, Alexander, Roosing, Susanne
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Elsevier 2021
Materias:
Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8756506/
https://www.ncbi.nlm.nih.gov/pubmed/35047838
http://dx.doi.org/10.1016/j.xhgg.2021.100046

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8756506/
https://www.ncbi.nlm.nih.gov/pubmed/35047838
http://dx.doi.org/10.1016/j.xhgg.2021.100046

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