Tamary H, Klinger G, Shalmon L, Attias D, Fortina P, Kobayashi M, Surrey S, Zaizov R
Department of Pediatric Hematology/Oncology Schneider Children's Medical Center of Israel, Petah Tiqva, Israel.
Hemoglobin. 1997 Mar;21(2):121-30. doi: 10.3109/03630269708997516.
We have identified a 16 bp deletion in the 3' untranslated region of the alpha 2-globin gene, including the first nucleotide of the polyadenylation signal sequence. The propositus, her mother and one of her brothers, all heterozygotes for the above deletion, have mild microcytic anemia. This is the first description of a deletion in the alpha gene involving both the 3' untranslated region and the polyadenylation signal sequence, causing alpha-thalassemia.
我们在α2-珠蛋白基因的3'非翻译区鉴定出一个16bp的缺失,包括聚腺苷酸化信号序列的第一个核苷酸。先证者、她的母亲和她的一个兄弟都是上述缺失的杂合子,均患有轻度小细胞贫血。这是首次描述涉及3'非翻译区和聚腺苷酸化信号序列的α基因缺失导致α地中海贫血。