Hemoglobin A2 (HbA2) has a measure of unreliability in diagnosing β-thalassemia trait (β-TT)

Autor:	Sayed AbdulAzeez, Noor B. Almandil, Zaki A. Naserullah, Mohammed Shakil Akhtar, Amani M. Al-Amodi, Neda Z. Ghanem, Nazish Rafique Ahmed, Sana Al-Jarrash, Lubna Ibrahim Al Asoom, Amein K. Al-Ali, Sumayh A Aldakeel, J. Francis Borgio
Rok vydání:	2018
Předmět:	Genetics Globin genes business.industry General Medicine 03 medical and health sciences 0302 clinical medicine Hemoglobin A2 030220 oncology & carcinogenesis Mutation (genetic algorithm) Trait Medicine business β thalassemia trait 030215 immunology
Zdroj:	Current Medical Research and Opinion. 34:945-951
ISSN:	1473-4877 0300-7995
Popis:	Introduction: Detection of β-thalassemia trait or carriers (β-TT) depends significantly on an increase in Hemoglobin A2 (HbA2) levels, which is found at low levels (
Databáze:	OpenAIRE
Externí odkaz:	https://explore.openaire.eu/search/publication?articleId=doi_________::b014a04cf61ad60e66bcd9c7434eab8f https://doi.org/10.1080/03007995.2018.1435520 Zobrazit plný text záznamu