BTKbase, mutation database for X-linked agammaglobulinemia (XLA).
X-linked agammaglobulinemia (XLA) is an immunodeficiency caused by mutations in the gene coding for Bruton's agammaglobulinemia tyrosine kinase (BTK). A database (BTKbase) of BTK mutations has been compiled and the recent update lists 463 mutation entries from 406 unrelated families showing 303 uniq...
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| Publicat a: | Nucleic Acids Res |
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| Autors principals: | , , , , , , , , , , , , |
| Format: | Artigo |
| Idioma: | Inglês |
| Publicat: |
Oxford University Press
1998
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| Matèries: | |
| Accés en línia: | https://ncbi.nlm.nih.govhttps://pmc.ncbi.nlm.nih.gov/articles/PMC147244/ https://ncbi.nlm.nih.govhttps://pubmed.ncbi.nlm.nih.gov/9399844/ https://ncbi.nlm.nih.govhttps://doi.org/10.1093/nar/26.1.242 |
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