Codi QR

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...

Descripció completa

Guardat en:
Dades bibliogràfiques
Publicat a:Nucleic Acids Res
Autors principals: Vihinen, M, Brandau, O, Brandén, L J, Kwan, S P, Lappalainen, I, Lester, T, Noordzij, J G, Ochs, H D, Ollila, J, Pienaar, S M, Riikonen, P, Saha, B K, Smith, C I
Format: Artigo
Idioma:Inglês
Publicat: Oxford University Press 1998
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
Etiquetes: Afegir etiqueta
Sense etiquetes, Sigues el primer a etiquetar aquest registre!