Three Mexican Families with β thalassemia intermedia with different molecular basis

Beta thalassemia (β-thal) is a frequent monogenic disease, is clinically and molecularly heterogeneous. This study described molecular and laboratory findings for three Mexican patients with β-thal intermedia phenotype and their relatives. Three Mexican families were studied for presenting β-thal in...

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Dades bibliogràfiques
Publicat a:Genet Mol Biol
Autors principals: de la Torre, Lourdes del Carmen Rizo, Díaz, Francisco Javier Perea, Cortés, Bertha Ibarra, López, Víctor Manuel Rentería, López, Josefina Yoaly Sánchez, Anzaldo, Francisco Javier Sánchez, Torres, María Teresa Magaña, Gonnet, Katia, Badens, Catherine, Bonello-Palot, Nathalie
Format: Artigo
Idioma:Inglês
Publicat: Sociedade Brasileira de Genética 2020
Matèries:
Human and Medical Genetics
Accés en línia:https://ncbi.nlm.nih.gov/pmc/articles/PMC7198011/
https://ncbi.nlm.nih.gov/pubmed/32142096
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1590/1678-4685-GMB-2019-0032
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