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Year | Number of Results |
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1985 | 1 |
1994 | 1 |
1999 | 2 |
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PubMed (cited) for id: 604571
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A subject with a novel type I bare lymphocyte syndrome has tapasin deficiency due to deletion of 4 exons by Alu-mediated recombination.
Blood. 2002 Aug 15;100(4):1496-8. doi: 10.1182/blood-2001-12-0252.
Blood. 2002.
PMID: 12149238
Free article.
Association of a syndrome resembling Wegener's granulomatosis with low surface expression of HLA class-I molecules.
Moins-Teisserenc HT, Gadola SD, Cella M, Dunbar PR, Exley A, Blake N, Baykal C, Lambert J, Bigliardi P, Willemsen M, Jones M, Buechner S, Colonna M, Gross WL, Cerundolo V.
Moins-Teisserenc HT, et al.
Lancet. 1999 Nov 6;354(9190):1598-603. doi: 10.1016/s0140-6736(99)04206-3.
Lancet. 1999.
PMID: 10560675
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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.
Furukawa H, et al.
J Clin Invest. 1999 Mar;103(5):755-8. doi: 10.1172/JCI5335.
J Clin Invest. 1999.
PMID: 10074494
Free PMC article.
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Homozygous human TAP peptide transporter mutation in HLA class I deficiency.
de la Salle H, Hanau D, Fricker D, Urlacher A, Kelly A, Salamero J, Powis SH, Donato L, Bausinger H, Laforet M, et al.
de la Salle H, et al.
Science. 1994 Jul 8;265(5169):237-41. doi: 10.1126/science.7517574.
Science. 1994.
PMID: 7517574
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Defective expression of HLA class I antigens: a case of the bare lymphocyte without immunodeficiency.
Maeda H, Hirata R, Chen RF, Suzaki H, Kudoh S, Tohyama H.
Maeda H, et al.
Immunogenetics. 1985;21(6):549-58. doi: 10.1007/BF00395879.
Immunogenetics. 1985.
PMID: 3891604
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