Isolation of the defective gene in X linked agammaglobulinaemia.

Author:

Vetrie D

Publisher

BMJ

Subject

Genetics (clinical),Genetics

Reference25 articles.

1. Isolation of a candidate gene for Menkes disease and evidence that it encodes a copper-transporting ATPase;Vulpe, C.; Levinson, B.; Whitney, S.; Packman, S.; Gitschier, J.;Nature Genet,1993

2. Isolation of a candidate gene for Menkes disease that encodes a potential heavy metal binding protein;Chelly, J.; Tumer, Z.; Tonnesen, T.;Nature Genet,1993

3. Isolation of a partial candidate gene for Menkes disease by positional cloning;Mercer, J.; Livingston, J.; Hall, B.;Nature Genet,1993

4. The CD40 ligand, gp39, is defective in activated T cells from patients with X-linked hyper-IgM syndrome;Aruffo, A.; Farrington, M.; Hollenbaugh, D.;Cell,1993

5. CD40 ligand gene defects responsible for X-linked hyper-IgM syndrome;Allen, R.C.; Armitage, R.J.; Conley, M.E.;Science,1993

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