Alpha thalassemia and alpha-MRE haplotypes in Uruguayan patients with microcytosis and hypochromia without anemia

Alpha thalassemia is the most common genetic disorder across the world, being the α-(3.7) deletion the most frequent mutation. In order to analyze the spectrum and origin of alpha thalassemia mutations in Uruguay, we obtained a sample of 168 unrelated outpatients with normal hemoglobin levels with m...

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Detalles Bibliográficos
Autores principales: Soler, Ana María, Piellusch, Bruna Facanali, da Silveira, Lorena, Pedroso, Gisele Audrei, López, Pablo, Savio, Enrique, Sonati, María de Fatima, da Luz, Julio
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Sociedade Brasileira de Genética 2021
Materias:
Human and Medical Genetics
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7995682/
https://www.ncbi.nlm.nih.gov/pubmed/33769430
http://dx.doi.org/10.1590/1678-4685-GMB-2020-0399

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7995682/
https://www.ncbi.nlm.nih.gov/pubmed/33769430
http://dx.doi.org/10.1590/1678-4685-GMB-2020-0399

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