[1] 杰夫·丹尼尔. 人类血型[M].中译版.北京:科学出版社,2007:327-351. [2] Singleton BK, Burton NM, Green C, et al. Mutations in EKLF/KLF1 form the molecular basis of the rare blood group In(Lu) phenotype[J]. Blood,2008,112(5):2081-2088. [3] Daniels G. Lutheran[J]. Immunohematology,2009,25 (4):152-159. [4] 焦 伟,黎海澜,王 晨,等. 广西壮族人群稀有血型筛选[J]. 现代免疫学,2011,31 (5):401-404. [5] 朱自严,沈 伟,陈和平,等.上海地区部分人群Jk(a-b-)、Dib-、Wrb-、K0、Ena-、Tja-、Ge-稀有血型筛选[J]. 中国输血杂志,2002,15 (4):232-233. [6] 中华人民共和国卫生部.中国输血技术手册(血站部分)[M].天津:科学技术出版社,1997:79-81. [7] 王 晨,李 勤,朱自严,等.中国稀有Lu-(null)血型筛查及其LU基因检测[J]. 中国输血杂志,2012,25(S1):129. [8] Gallienne AE, Dréau HM, Schuh A, et al. Ten novel mutations in the erythroid transcription factor KLF1 gene associated with increased fetal hemoglobin levels in adults[J]. Haematologica,2012,97 (3):340-343. [9] Singleton BK, Lau W, Fairweather VS,et al. Mutations in the second zinc finger of human EKLF reduce promoter affinity but give rise to benign and disease phenotypes[J]. Blood,2011,118 (11):3137-3145. [10] Singleton BK, Frayne J, Anstee DJ, et al. Blood group phenotypes resulting from mutations in erythroid transcription factors[J]. Curr Opin Hematol,2012,19 (6):486-493. |