Corrons, Garcia, Tusell, Varughese, West, Beutler: "Red cell adenylate kinase deficiency: molecular study of 3 new mutations (118G>A, 190G>A, and GAC deletion) associated with hereditary nonspherocytic hemolytic anemia." in: Blood, Vol. 102, Issue 1, pp. 353-6, 2003 (PubMed).
Toren, Brok-Simoni, Ben-Bassat, Holtzman, Mandel, Neumann, Ramot, Rechavi, Kende: "Congenital haemolytic anaemia associated with adenylate kinase deficiency." in: British journal of haematology, Vol. 87, Issue 2, pp. 376-80, 1994 (PubMed).
Matsuura, Igarashi, Tanizawa, Yamada, Kishi, Kajii, Fujii, Miwa, Sakurai, Nakazawa: "Human adenylate kinase deficiency associated with hemolytic anemia. A single base substitution affecting solubility and catalytic activity of the cytosolic adenylate kinase." in: The Journal of biological chemistry, Vol. 264, Issue 17, pp. 10148-55, 1989 (PubMed).
Zuffardi, Caiulo, Maraschio, Tupler, Bianchi, Amisano, Beluffi, Moratti, Liguri: "Regional assignment of the loci for adenylate kinase to 9q32 and for alpha 1-acid glycoprotein to 9q31-q32. A locus for Goltz syndrome in region 9q32-qter?" in: Human genetics, Vol. 82, Issue 1, pp. 17-9, 1989 (PubMed).
Miwa, Fujii, Tani, Takahashi, Takizawa, Igarashi: "Red cell adenylate kinase deficiency associated with hereditary nonspherocytic hemolytic anemia: clinical and biochemical studies." in: American journal of hematology, Vol. 14, Issue 4, pp. 325-33, 1983 (PubMed).