Linkage of familial hemophagocytic lymphohistiocytosis to 10q21-22 and evidence for heterogeneity.

Familial hemophagocytic lymphohistiocytosis (FHL) is an autosomal recessive disorder characterized by the early onset of overwhelming activation of T lymphocytes and macrophages, invariably leading to death, in the absence of allogeneic bone marrow transplantation. Using genomewide genetic linkage a...

Täydet tiedot

Tallennettuna:
Bibliografiset tiedot
Päätekijät: Dufourcq-Lagelouse, R, Jabado, N, Le Deist, F, Stéphan, J L, Souillet, G, Bruin, M, Vilmer, E, Schneider, M, Janka, G, Fischer, A, de Saint Basile, G
Aineistotyyppi: Artigo
Kieli:Inglês
Julkaistu: 1999
Aiheet:
Research Article
Linkit:https://ncbi.nlm.nih.gov/pmc/articles/PMC1377715/
https://ncbi.nlm.nih.gov/pubmed/9915956
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