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Hemoglobin calabria leading to undetectable hemoglobin A1C

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dc.contributor.authorUyanık, Bülent
dc.contributor.institutionauthorUYANIK, BÜLENT
dc.date.accessioned2021-01-27T20:59:22Z
dc.date.available2021-01-27T20:59:22Z
dc.date.issued2019-07-01T00:00:00Z
dc.description.abstractMore than 12,000 hemoglobin (Hb) variants have been identified and listed on the HbVar database. Reliable detection of these Hb variants is important for planning hemoglobinopathy screening and genetic counseling. Presumptive diagnosis is usually dependent on dedicated Hb analyzers, e.g. high-performance liquid chromatography (HPLC) or capillary electrophoresis (CE) systems specifically developed for Hb fraction separation and quantification. In most cases, simple Hb variants can be easily identified. Rarely, a novel Hb molecule formed by the assembly of different defective globin chains could complicate clinical and laboratory diagnostics and requires DNA testing
dc.identifier.citationUyanık B., -Hemoglobin calabria leading to undetectable hemoglobin A1C-, Internal Medicine and Care, cilt.3, ss.1-2, 2019
dc.identifier.doi10.15761/imc.1000131
dc.identifier.urihttp://hdl.handle.net/20.500.12645/28190
dc.rightsinfo:eu-repo/semantics/openAccess
dc.titleHemoglobin calabria leading to undetectable hemoglobin A1C
dc.typeArticle
dspace.entity.typePublication
local.avesis.id92596e8f-64ab-482e-b457-4abf7f43207b
local.publication.isinternational1
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