Three Mexican Families with β thalassemia intermedia with different molecular basis

Autor: Torre Ldcr, Badens C, López Vmr, Gonnet K, Díaz Fjp, López Jys, Cortés Bi, Anzaldo Fjs, Bonello-Palot N, Torres Mtm

Publikováno v: Genetics and Molecular Biology, Vol 42, Iss 4 (2020)
Genetics and Molecular Biology v.42 n.4 2019
Genetics and Molecular Biology
Sociedade Brasileira de Genética (SBG)
instacron:SBG

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 Me

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::76740c4c5a511af49bd3467db8ce32a0
http://www.scielo.br/pdf/gmb/v42n4/1415-4757-GMB-42-4-e20190032.pdf