1、 KORNSTAD L. A rare blood group antigen, Ola (Oldeide), associated with weak Rh antigens[J]. Vox Sang,1986,50(4): 235-239. KORNSTAD L. A rare blood group antigen, Ola (Oldeide), associated with weak Rh antigens[J]. Vox Sang,1986,50(4): 235-239.
2、 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. 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.
3、 GENETET S,RIPOCHE P,PICOT J,et al. Human RhAG ammonia channel is impaired by the Phe65Ser mutation in overhydrated stomatocytic red cells[J]. Am J Physiol Cell Physiol,2012,302(2): C419-C428. GENETET S,RIPOCHE P,PICOT J,et al. Human RhAG ammonia channel is impaired by the Phe65Ser mutation in overhydrated stomatocytic red cells[J]. Am J Physiol Cell Physiol,2012,302(2): C419-C428.
4、 HUANG C,CHENG G J,REID M E,et al. Rhmod syndrome: a family study of the translation-initiator mutation in the Rh50 glycoprotein gene[J]. Am J Hum Genet,1999,64(1): 108-117. HUANG C,CHENG G J,REID M E,et al. Rhmod syndrome: a family study of the translation-initiator mutation in the Rh50 glycoprotein gene[J]. Am J Hum Genet,1999,64(1): 108-117.
5、 HUANG C H,CHENG G,LIU Z,et al. Molecular basis for Rh null syndrome: Identification of three new missense mutations in the Rh50 glycoprotein gene[J]. Am J Hematol,1999,62(1): 25-32. HUANG C H,CHENG G,LIU Z,et al. Molecular basis for Rh null syndrome: Identification of three new missense mutations in the Rh50 glycoprotein gene[J]. Am J Hematol,1999,62(1): 25-32.
6、 FLEGEL W A. Molecular genetics and clinical applications for RH[J]. TRANSFUS APHER SCI,2011,44(1): 81-91. FLEGEL W A. Molecular genetics and clinical applications for RH[J]. TRANSFUS APHER SCI,2011,44(1): 81-91.
7、 TIAN L,SONG N,YAO Z Q,et al. A family study of the Chinese Rhnull individual of the regulator type: a novel single missense mutation identified in RHAG gene[J]. Transfsion, 2011, 51(12):2686-2689. TIAN L,SONG N,YAO Z Q,et al. A family study of the Chinese Rhnull individual of the regulator type: a novel single missense mutation identified in RHAG gene[J]. Transfsion, 2011, 51(12):2686-2689.
8、 MATASSI G, Chérifzahar B, RAYNAL V, et al. Organization of the human RH50 A gene(RHAG) and evolution of base composltlon of the RH gene family[J]. Genomics,1998,47(2):286-293. MATASSI G, Chérifzahar B, RAYNAL V, et al. Organization of the human RH50 A gene(RHAG) and evolution of base composltlon of the RH gene family[J]. Genomics,1998,47(2):286-293.
9、 HUANG C H. The human RH50 glycoprotein gene[J]. J Biol Chem 1998,273(4):2207-2213. HUANG C H. The human RH50 glycoprotein gene[J]. J Biol Chem 1998,273(4):2207-2213.
10、 TILLEY L, GREEN C, POOLE J, et al. A new blood group system, RHAG: three antigens resulting from amino acid substitutions in the Rh-associated glycoprotein[J]. Vox Sanguinis,2010,98(2):151-159. TILLEY L, GREEN C, POOLE J, et al. A new blood group system, RHAG: three antigens resulting from amino acid substitutions in the Rh-associated glycoprotein[J]. Vox Sanguinis,2010,98(2):151-159.
