Citations for

1	XIAP, XLP2
	Symptomatic males and female carriers in a large Caucasian kindred with XIAP deficiency.
	Dziadzio M, Ammann S, Canning C, Boyle F, Hassan A, Cale C, Elawad M, Fiil BK, Gyrd-Hansen M, Salzer U, Speckmann C, Grimbacher B.
	J Clin Immunol 35(5):439-44. doi: 10.1007/s10875-015-0166-0. Epub 2015 May 6. 2015
2	LYP, SH2D1A, XIAP, XLP2
	Clinical similarities and differences of patients with X-linked lymphoproliferative syndrome type 1 (XLP-1/SAP deficiency) versus type 2 (XLP-2/XIAP deficiency).
	Pachlopnik Schmid J, Canioni D, Moshous D, Touzot F, Mahlaoui N, Hauck F, Kanegane H, Lopez-Granados E, Mejstrikova E, Pellier I, Galicier L, Galambrun C, Barlogis V, Bordigoni P, Fourmaintraux A, Hamidou M, Dabadie A, Le Deist F, Haerynck F, Ouachée-Chardin M, Rohrlich P, Stephan JL, Lenoir C, Rigaud S, Lambert N, Milili M, Schiff C, Chapel H, Picard C, de Saint Basile G, Blanche S, Fischer A, Latour S.
	Blood 117(5):1522-9. Epub 2010 Nov 30. 2011
3	LYP, XIAP, XLP2
	XIAP deficiency in humans causes an X-linked lymphoproliferative syndrome.
	Rigaud S, Fondaneche MC, Lambert N, Pasquier B, Mateo V, Soulas P, Galicier L, Le Deist F, Rieux-Laucat F, Revy P, Fischer A, de Saint Basile G, Latour S.
	Nature 444(7115):110-4. 2006