Mapping of the X linked form of hyper IgM syndrome (HIGM1)

X linked immunodeficiency with hyperimmunoglobulinaemia M (HIGM1), which is characterised by agammaglobulinaemia together with excess IgM production reflecting an impairment of the immunoglobulin heavy chain class switch of B lymphocytes, has been mapped to Xq26. We report multipoint linkage data in...

Täydet tiedot

Tallennettuna:
Bibliografiset tiedot
Julkaisussa:J Med Genet
Päätekijät: Padayachee, M, Levinsky, R J, Kinnon, C, Finn, A, McKeown, C, Feighery, C, Notarangelo, L D, Hendriks, R W, Read, A P, Malcolm, S
Aineistotyyppi: Artigo
Kieli:Inglês
Julkaistu: BMJ Publishing Group 1993
Aiheet:
Research Article
Linkit:https://ncbi.nlm.nih.govhttps://pmc.ncbi.nlm.nih.gov/articles/PMC1016299/
https://ncbi.nlm.nih.govhttps://pubmed.ncbi.nlm.nih.gov/8097258/
https://ncbi.nlm.nih.govhttps://doi.org/10.1136/jmg.30.3.202
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