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4 results on '"Vihinen M"'

1. BTKbase: XLA-mutation registry

Author

Vihinen, M., Brooimans, Ra, Kwan, Sp, Lehvaslaiho, H., Litman, Gw, Ochs, Hd, Resnick, I., Schwaber, Jh, Vorchovsky, I., and C. I. Edvard SMITH

Subjects
Immunology
Published
1996
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3. CD40lbase: a database of CD40L gene mutations causing X-linked hyper-IgM syndrome.

Author

Notarangelo LD, Peitsch MC, Abrahamsen TG, Bachelot C, Bordigoni P, Cant AJ, Chapel H, Clementi M, Deacock S, de Saint Basile G, Duse M, Espanol T, Etzioni A, Fasth A, Fischer A, Giliani S, Gomez L, Hammarstorm L, Jones A, Kanariou M, Kinnon C, Klemola T, Kroczek RA, Levy J, Matamoros N, Monafo V, Paolucci P, Reznick I, Sanal O, Smith CI, Thompson RA, Tovo P, Villa A, Vihinen M, Vossen J, and Zegers BJ

Subjects
CD40 Ligand, Genetic Linkage, Humans, Ligands, CD40 Antigens genetics, Databases, Factual, Hypergammaglobulinemia genetics, Immunoglobulin M genetics, Membrane Glycoproteins genetics, Mutation, X Chromosome
Abstract

X-linked hyper-IgM syndrome (X-HIM) is an immunodeficiency caused by mutations in the gene encoding the CD40 ligand (CD40L). A database (CD40Lbase) of CD40L mutations has now been established, and the resultant information, together with other mutations reported elsewhere in the literature, is presented here.

Published
1996
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