FOXP3 forkhead domain mutation and regulatory T cells in the IPEX syndrome.

Authors :: d'Hennezel E
Ben-Shoshan M
Ochs HD
Torgerson TR
Russell LJ
Lejtenyi C
Noya FJ
Jabado N
Mazer B
Piccirillo CA
Source :: The New England journal of medicine [N Engl J Med] 2009 Oct 22; Vol. 361 (17), pp. 1710-3.
Publication Year :: 2009

Subjects :: Abnormalities, Multiple immunology
Autoimmune Diseases genetics
Fatal Outcome
Forkhead Transcription Factors metabolism
Gene Expression Regulation
Humans
Infant, Newborn
Infant, Premature
Intestinal Diseases immunology
Male
Phenotype
Polyendocrinopathies, Autoimmune immunology
Syndrome
Abnormalities, Multiple genetics
Forkhead Transcription Factors genetics
Intestinal Diseases genetics
Mutation, Missense
Polyendocrinopathies, Autoimmune genetics
T-Lymphocytes, Regulatory

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