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Hyperhaemolysis in a pregnant woman with a homozygous β(0)‐thalassemia mutation and two genetic modifiers
INTRODUCTION: Patients with a homozygous β(0)‐thalassemia mutation usually have a transfusion‐dependent β‐thalassemia major phenotype. However, some β‐thalassemia patients present with a relatively mild and even normal phenotype and always have a high level of Hb F induced by genetic modifiers. METH...
| Autores principales: | , , , , |
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| Formato: | Online Artículo Texto |
| Lenguaje: | English |
| Publicado: |
John Wiley and Sons Inc.
2021
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| Materias: | |
| Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8372088/ https://www.ncbi.nlm.nih.gov/pubmed/33960744 http://dx.doi.org/10.1002/mgg3.1696 |