TAP1base mutation publications [2006] [2005] [1999] Search PubMed latest citations for TAP1 mutations 2006 A novel mutation for TAP deficiency and its possible association with Toxoplasmosis. Doğu F, Ikincioğullari A, Fricker D, Bozdoğan G, Aytekin C, Ileri M, Teziç T, Babacan E, De La Salle H Parasitol Int 2006(3): 219-22 [PubMed abstract]. 2005 Unilateral necrotising toxoplasmic retinochoroiditis as the main clinical manifestation of a peptide transporter (TAP) deficiency. Parissiadis A, Dormoy A, Fricker D, Hanau D, de la Salle H, Cazenave JP, Lenoble P, Donato L Br J Ophthalmol 2005(12): 1661-2 [PubMed abstract]. 1999 HLA class I deficiencies due to mutations in subunit 1 of the peptide transporter TAP1. de la Salle H, Zimmer J, Fricker D, Angenieux C, Cazenave JP, Okubo M, Maeda H, Plebani A, Tongio MM, Dormoy A, Hanau D J Clin Invest 1999(5): R9-R13 [PubMed abstract]. Splice acceptor site mutation of the transporter associated with antigen processing-1 gene in human bare lymphocyte syndrome. Furukawa H, Murata S, Yabe T, Shimbara N, Keicho N, Kashiwase K, Watanabe K, Ishikawa Y, Akaza T, Tadokoro K, Tohma S, Inoue T, Tokunaga K, Yamamoto K, Tanaka K, Juji T J Clin Invest 1999(5): 755-8 [PubMed abstract].