| 1 | CD59, CD59D |
| CD59 deficiency is associated with chronic hemolysis and childhood relapsing immune mediated polyneuropathy. | |
| Nevo Y, Ben-Zeev B, Tabib A, Straussberg R, Anikster Y, Shorer Z, Fattal-Valevski A, Ta-Shma A, Aharoni S, Rabie M, Zenvirt S, Goldshmidt H, Fellig Y, Shaag A, Mevorach D, Elpeleg O. | |
| Blood lood. 2012 Nov 13. [Epub ahead of print] 2012 | |
| 2 | CD59, CD59D |
| Targeted deletion of the CD59 gene causes spontaneous intravascular hemolysis and hemoglobinuria. | |
| Holt DS, Botto M, Bygrave AE, Hanna SM, Walport MJ, Morgan BP. | |
| Blood 98(2):442-9. 2001 | |
| 3 | CD59, CD59D, PIGA, PNH |
| CD59-deficient blood cells and PIG-A gene abnormalities in Japanese patients with aplastic anaemia. | |
| Azenishi Y, et al. | |
| Br J Haematol 104(3):523-9. 1999 | |
| 4 | CD59, CD59D |
| Paroxysmal nocturnal hemoglobinuria due to hereditary nucleotide deletion in the HRF20 (CD59) gene. | |
| Motoyama N, et al. | |
| Eur J Immunol 22 : 2669-2673. 1992 | |
| 5 | CD59, CD59D, PNH |
| Inherited complete deficiency of 20-kilodalton homologous restriction factor (CD59) as a cause of paroxysmal nocturnal hemoglobinuria. | |
| Yamashina M, et al. | |
| N Engl J Med 323 : 1184-1189. 1990 | |