Cargando…
Enabling routine β-thalassemia Prevention and Patient Management by scalable, combined Thalassemia and Hemochromatosis Mutation Analysis
BACKGROUND: Beta (β)-thalassemia is one of the most common inherited disorders worldwide, with high prevalence in the Mediterranean, the Middle East and South Asia. Over the past 40 years, awareness and prevention campaigns in many countries have greatly reduced the incidence of affected child birth...
Autores principales: | Hashmi, Ghazala, Qidwai, Asim, Fernandez, Kristopher, Seul, Michael |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2020
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7229588/ https://www.ncbi.nlm.nih.gov/pubmed/32414341 http://dx.doi.org/10.1186/s12881-020-01017-x |
Ejemplares similares
-
New thiazolidinones reduce iron overload in mouse models of hereditary hemochromatosis and β-thalassemia
por: Liu, Jing, et al.
Publicado: (2019) -
Hemochromatosis in a β‐thalassemia minor patient with H63D homozygous mutation: A case report
por: Pokhrel, Nishan Babu, et al.
Publicado: (2020) -
Analysis of Common Beta-Thalassemia (β-Thalassemia) Mutations in East Java, Indonesia
por: Hernaningsih, Yetti, et al.
Publicado: (2022) -
Late-onset Hemochromatosis: Co-inheritance of β-thalassemia and Hereditary Hemochromatosis in a Chinese Family: A Case Report and Epidemiological Analysis of Diverse Populations
por: Yang, Jinjun, et al.
Publicado: (2017) -
β-Thalassemia Mutations among Transfusion-Dependent Thalassemia Major Patients in Northern Iraq
por: Al-Allawi, Nasir A. S., et al.
Publicado: (2010)