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Primary immunodeficiency mutation databases.
Vihinen M, Arredondo-Vega FX, Casanova JL, Etzioni A, Giliani S, Hammarström L, Hershfield MS, Heyworth PG, Hsu AP, Lähdesmäki A, Lappalainen I, Notarangelo LD, Puck JM, Reith W, Roos D, Schumacher RF, Schwarz K, Vezzoni P, Villa A, Väliaho J, Smith CI. Vihinen M, et al. Among authors: lappalainen i. Adv Genet. 2001;43:103-88. doi: 10.1016/s0065-2660(01)43005-7. Adv Genet. 2001. PMID: 11037300 Review.
Registries of immunodeficiency patients and mutations.
Lappalainen I, Ollila J, Smith CI, Vihinen M. Lappalainen I, et al. Hum Mutat. 1997;10(4):261-7. doi: 10.1002/(SICI)1098-1004(1997)10:4<261::AID-HUMU1>3.0.CO;2-K. Hum Mutat. 1997. PMID: 9338579 Review.
Sequence specificity in CpG mutation hotspots.
Ollila J, Lappalainen I, Vihinen M. Ollila J, et al. Among authors: lappalainen i. FEBS Lett. 1996 Nov 4;396(2-3):119-22. doi: 10.1016/0014-5793(96)01075-7. FEBS Lett. 1996. PMID: 8914970 Free article.
BTKbase, mutation database for X-linked agammaglobulinemia (XLA).
Vihinen M, Belohradsky BH, Haire RN, Holinski-Feder E, Kwan SP, Lappalainen I, Lehväslaiho H, Lester T, Meindl A, Ochs HD, Ollila J, Vorechovsky I, Weiss M, Smith CI. Vihinen M, et al. Among authors: lappalainen i. Nucleic Acids Res. 1997 Jan 1;25(1):166-71. doi: 10.1093/nar/25.1.166. Nucleic Acids Res. 1997. PMID: 9016530 Free PMC article.
BTKbase, mutation database for X-linked agammaglobulinemia (XLA).
Vihinen M, Brandau O, Brandén LJ, Kwan SP, Lappalainen I, Lester T, Noordzij JG, Ochs HD, Ollila J, Pienaar SM, Riikonen P, Saha BK, Smith CI. Vihinen M, et al. Among authors: lappalainen i. Nucleic Acids Res. 1998 Jan 1;26(1):242-7. doi: 10.1093/nar/26.1.242. Nucleic Acids Res. 1998. PMID: 9399844 Free PMC article.
30 results