Zobrazeno 1 - 1
of 1
pro vyhledávání: '"betha thalassemia"'
Autor:
Blanca Issé, Myriam E. Ledesma Achem, Sandra Stella Lazarte, Ana Cecilia Haro, Maria Eugenia Monaco, Cecilia Jiménez
Publikováno v:
Hemoglobin. 38:394-401
The main hereditary hemoglobin (Hb) disorder in Argentina is b-thalassemia (b-thal). Molecular studies performed in the center of the country exhibited a marked prevalence of the codon 39 (C4T) and IVS-I-110 (G4A) mutations. The northwest region of A
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::21aa6262bea67b120b20c6b18fb7ce08
https://doi.org/10.3109/03630269.2014.968784
https://doi.org/10.3109/03630269.2014.968784
