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...

Descripción completa

Detalles Bibliográficos
Autores principales: 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
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Sociedade Brasileira de Genética 2020
Materias:
Human and Medical Genetics
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7198011/
https://www.ncbi.nlm.nih.gov/pubmed/32142096
http://dx.doi.org/10.1590/1678-4685-GMB-2019-0032

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7198011/
https://www.ncbi.nlm.nih.gov/pubmed/32142096
http://dx.doi.org/10.1590/1678-4685-GMB-2019-0032

Ejemplares similares