| Literature DB >> 23718193 |
Gareth Gerrard1, Mikel Valgañón, Hui En Foong, Dalia Kasperaviciute, Deena Iskander, Laurence Game, Michael Müller, Timothy J Aitman, Irene Roberts, Josu de la Fuente, Letizia Foroni, Anastasios Karadimitris.
Abstract
Diamond-Blackfan anaemia (DBA) is caused by inactivating mutations in ribosomal protein (RP) genes, with mutations in 13 of the 80 RP genes accounting for 50-60% of cases. The remaining 40-50% cases may harbour mutations in one of the remaining RP genes, but the very low frequencies render conventional genetic screening as challenging. We, therefore, applied custom enrichment technology combined with high-throughput sequencing to screen all 80 RP genes. Using this approach, we identified and validated inactivating mutations in 15/17 (88%) DBA patients. Target enrichment combined with high-throughput sequencing is a robust and improved methodology for the genetic diagnosis of DBA.Entities:
Keywords: Diamond-Blackfan anaemia; molecular diagnostics; next generation sequencing; target enrichment
Mesh:
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Year: 2013 PMID: 23718193 DOI: 10.1111/bjh.12397
Source DB: PubMed Journal: Br J Haematol ISSN: 0007-1048 Impact factor: 6.998