[1] WAGNER F F,FLEGEL W A.Review: the molecular basis of the Rh blood group phenotypes[J].Immunohematology,2004,20(1):23-36. [2] 杰夫.丹尼尔. 人类血型[M]. 北京:科学出版社,2007,281. [3] 王鹤,李树中,李中华,等.RHAG血型抗原研究进展[J].临床血液学杂志(输血与检验),2019,32(6):479-482. [4] XIA R W,XUN C Z,XIANG D,et al.A novel double-variant RHAG allele leads to Rhmod phenotype[J].Transfus Med,2019,29(6):460-465. [5] MU S,CUI Y,WANG W,et al.A RHAG point mutation selectively disrupts Rh antigen expression[J].Transfus Med,2019,29(2):121-127. [6] POLIN H,PELC-KLOPOTOWSKA M,DANZER M,et al.Compound heterozygosity of two novel RHAG alleles leads to a considerable disruption of the Rh complex[J].Transfusion,2016,56(4):950-955. [7] USHIKI T,TSUNEYAMA H,MASUKO M,et al.Rhnull phenotype caused by a novel RHAG mutation,c.945+1G>A,in the Japanese population[J].Transfusion,2019,59(8):2519-2522. [8] TIAN L,XU H,XIAO J,et al.A novel nucleotide deletion in RHAG allele identified in a Chinese Rhnull individual[J].Transfusion,2018,58(3):826-827. [9] 王群,李剑平.Rhnull综合征的分子遗传学研究[J].中国输血杂志,2008,21(2):133-135. [10] 吴大洲,左琴琴,王满妮,等.RHAG 236G>A突变致Rhmod的分子背景研究及家系调查[J].中国输血杂志,2015,28(7):757-759. [11] 陈文伟,邵超鹏.中国人群中RHAG基因序列的观察[J].广州医药,2018,49(1):9-12. [12] WEN J Z,VERHAGEN O J H M,JIA S S,et al.A variant RhAG protein encoded by theRHAG*572Aallele causes serological weak D expression while maintaining normal RhCE phenotypes[J].Transfusion,2019,59(1):405-411. |