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HBB mutations and HbA2 level: Escaping the carrier screening programs
HbA2 level alone for beta thalassemia trait may not be accurate and reliable even without iron deficiency so molecular genetic testing is important and should be considered for some individuals.
Autores principales: | , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
John Wiley and Sons Inc.
2020
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7869310/ https://www.ncbi.nlm.nih.gov/pubmed/33598281 http://dx.doi.org/10.1002/ccr3.3714 |
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author | Sharifi, Ameneh Mahdieh, Nejat |
author_facet | Sharifi, Ameneh Mahdieh, Nejat |
author_sort | Sharifi, Ameneh |
collection | PubMed |
description | HbA2 level alone for beta thalassemia trait may not be accurate and reliable even without iron deficiency so molecular genetic testing is important and should be considered for some individuals. |
format | Online Article Text |
id | pubmed-7869310 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | John Wiley and Sons Inc. |
record_format | MEDLINE/PubMed |
spelling | pubmed-78693102021-02-16 HBB mutations and HbA2 level: Escaping the carrier screening programs Sharifi, Ameneh Mahdieh, Nejat Clin Case Rep Case Reports HbA2 level alone for beta thalassemia trait may not be accurate and reliable even without iron deficiency so molecular genetic testing is important and should be considered for some individuals. John Wiley and Sons Inc. 2020-12-29 /pmc/articles/PMC7869310/ /pubmed/33598281 http://dx.doi.org/10.1002/ccr3.3714 Text en © 2020 The Authors. Clinical Case Reports published by John Wiley & Sons Ltd. This is an open access article under the terms of the http://creativecommons.org/licenses/by-nc-nd/4.0/ License, which permits use and distribution in any medium, provided the original work is properly cited, the use is non‐commercial and no modifications or adaptations are made. |
spellingShingle | Case Reports Sharifi, Ameneh Mahdieh, Nejat HBB mutations and HbA2 level: Escaping the carrier screening programs |
title |
HBB mutations and HbA2 level: Escaping the carrier screening programs |
title_full |
HBB mutations and HbA2 level: Escaping the carrier screening programs |
title_fullStr |
HBB mutations and HbA2 level: Escaping the carrier screening programs |
title_full_unstemmed |
HBB mutations and HbA2 level: Escaping the carrier screening programs |
title_short |
HBB mutations and HbA2 level: Escaping the carrier screening programs |
title_sort | hbb mutations and hba2 level: escaping the carrier screening programs |
topic | Case Reports |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7869310/ https://www.ncbi.nlm.nih.gov/pubmed/33598281 http://dx.doi.org/10.1002/ccr3.3714 |
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