How will next generation sequencing (NGS) improve the diagnosis of congenital hemolytic anemia?
- PMID: 32355712
- PMCID: PMC7186692
- DOI: 10.21037/atm.2020.02.151
How will next generation sequencing (NGS) improve the diagnosis of congenital hemolytic anemia?
Conflict of interest statement
Conflicts of Interest: The authors have no conflicts of interest to declare.
Comment on
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Clinical utility of targeted gene enrichment and sequencing technique in the diagnosis of adult hereditary spherocytosis.Ann Transl Med. 2019 Oct;7(20):527. doi: 10.21037/atm.2019.09.163. Ann Transl Med. 2019. PMID: 31807509 Free PMC article.
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- Bianchi P, Mohandas N. Hereditary disorders of the red cell membrane and disorders of red cell metabolism in Postgraduate Haematology. Hoffbrand AV, Higgs DR, Keeling DM, et al. editors. 7th edition. John Wiley & Sons, Ltd., 2016.
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- Zaninoni A, Fermo E, Vercellati C, et al. Use of Laser Assisted Optical Rotational Cell Analyzer (LoRRca MaxSis) in the Diagnosis of RBC Membrane Disorders, Enzyme Defects, and Congenital Dyserythropoietic Anemias: A Monocentric Study on 202 Patients. Front Physiol 2018;9:451. 10.3389/fphys.2018.00451 - DOI - PMC - PubMed
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