1. Hellberg A, Steffensen R, Yahalom V, Sojka BN, Heier HE, Levene C, et al. Additional molecular bases of the clinically important p blood group phenotype. Transfusion. 2003; 43:899–907. PMID:
12823750.
2. Koda Y, Soejima M, Sato H, Maeda Y, Kimura H. Three-base deletion and one-base insertion of the alpha(1,4)galactosyltransferase gene responsible for the P phenotype. Transfusion. 2002; 42:48–51. PMID:
11896312.
3. Hellberg A, Ringressi A, Yahalom V, Safwenberg J, Reid ME, Olsson ML. Genetic heterogeneity at the glycosyltransferase loci underlying the GLOB blood group system and collection. Br J Haematol. 2004; 125:528–536. PMID:
15142124.
4. Yan L, Zhu F, Xu X, Zantek ND. Molecular basis for p blood group phenotype in China. Transfusion. 2004; 44:136–138. PMID:
14692982.
5. Wang YC, Chang CF, Lin HC, Lin KS, Lin KT, Hung CM, et al. Functional characterisation of a complex mutation in the alpha(1,4)galactosyltransferase gene in Taiwanese individuals with p phenotype. Transfus Med. 2011; 21:84–89. PMID:
21092013.
6. Li X, Diao X, Xia X, Hong X, Zhu F. A novel mutation in
A4GALT was identified in a Chinese individual with p phenotype. Transfusion. 2017; 57:215–216. PMID:
27612185.
7. Fung MK EA, Spitalnik SL, et al. Technical Manual. 19th ed. Bethesda, Maryland: American Association of Blood Banks;2018. p. 286–290.
8. Matot I, Scheinin O, Jurim O, Eid A. Effectiveness of acute normovolemic hemodilution to minimize allogeneic blood transfusion in major liver resections. Anesthesiology. 2002; 97:794–800. PMID:
12357142.
9. Nadler SB, Hidalgo JH, Bloch T. Prediction of blood volume in normal human adults. Surgery. 1962; 51:224–232. PMID:
21936146.