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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Detalhes bibliográficos
Publicado no:Genet Mol Biol
Main Authors: 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: Artigo
Idioma:Inglês
Publicado em: Sociedade Brasileira de Genética 2020
Assuntos:
Human and Medical Genetics
Acesso em linha: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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