| 1 | IMD22, LCK |
| Primary T-cell immunodeficiency with immunodysregulation caused by autosomal recessive LCK deficiency. | |
| Hauck F, Randriamampita C, Martin E, Gerart S, Lambert N, Lim A, Soulier J, Maciorowski Z, Touzot F, Moshous D, Quartier P, Heritier S, Blanche S, Rieux-Laucat F, Brousse N, Callebaut I, Veillette A, Hivroz C, Fischer A, Latour S, Picard C. | |
| J Allergy Clin Immunol 130(5):1144-1152.e11. doi: 10.1016/j.jaci.2012.07.029. Epub 2012 Sep 15. 2012 | |
| 2 | IMD22, LCK |
| Defect of lck in a patient with common variable immunodeficiency. | |
| Sawabe T, Horiuchi T, Nakamura M, Tsukamoto H, Nakahara K, Harashima SI, Tsuchiya T, Nakano S. | |
| Int J Mol Med 7(6):609-14. 2001 | |