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Items: 5

1.

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.

Nucleic Acids Res. 1998 Jan 1;26(1):242-7.

2.

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.

Nucleic Acids Res. 1997 Jan 1;25(1):166-71. Erratum in: Nucleic Acids Res 1997 May 1;25(9):1874.

3.

BTKbase, mutation database for X-linked agammaglobulinemia (XLA).

Vihinen M, Iwata T, Kinnon C, Kwan SP, Ochs HD, Vorechovský I, Smith CI.

Nucleic Acids Res. 1996 Jan 1;24(1):160-5.

4.

Structural basis for chromosome X-linked agammaglobulinemia: a tyrosine kinase disease.

Vihinen M, Vetrie D, Maniar HS, Ochs HD, Zhu Q, Vorechovský I, Webster AD, Notarangelo LD, Nilsson L, Sowadski JM, et al.

Proc Natl Acad Sci U S A. 1994 Dec 20;91(26):12803-7.

5.

A new X linked recessive deafness syndrome with blindness, dystonia, fractures, and mental deficiency is linked to Xq22.

Tranebjaerg L, Schwartz C, Eriksen H, Andreasson S, Ponjavic V, Dahl A, Stevenson RE, May M, Arena F, Barker D, et al.

J Med Genet. 1995 Apr;32(4):257-63.

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