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Severe congenital hemolytic anemia caused by a novel compound heterozygous PKLR gene mutation in a Chinese boy
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作者 Peng-Peng Liu Hu-Qing Ding +2 位作者 shen-zhen huang Sheng-Yong Yang Ting Liu 《Chinese Medical Journal》 SCIE CAS CSCD 2019年第1期92-95,共4页
To the Editor:Congenital hemolytic anemia (CHA) can be caused by the defect of any component in red blood cell (RBC),including hemoglobinopathies,membrane and cytoskeleton defects,and metabolic enzymopathies etc.And i... To the Editor:Congenital hemolytic anemia (CHA) can be caused by the defect of any component in red blood cell (RBC),including hemoglobinopathies,membrane and cytoskeleton defects,and metabolic enzymopathies etc.And it is characterized by early present normocytic/macrocytic anemia,reticulocytosis,and elevated unconju-gated bilirubin. 展开更多
关键词 CHINESE BOY PKLR gene mutation SEVERE CONGENITAL HEMOLYTIC ANEMIA
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