FOXP3 forkhead domain mutation and regulatory T cells in the IPEX syndrome. The New England journal of medicine [N Engl J Med] Journal article | | Title | FOXP3 forkhead domain mutation and regulatory T cells in the IPEX syndrome. | | Author(s) | d'Hennezel E, Ben-Shoshan M, Ochs HD, Torgerson TR, Russell LJ, Lejtenyi C, Noya FJ, Jabado N, Mazer B, Piccirillo CA | | Source | N Engl J Med 2009 Oct 22; 361(17):1710-3. | | MeSH | Abnormalities, Multiple
Autoimmune Diseases
Fatal Outcome
Forkhead Transcription Factors
Gene Expression Regulation
Humans
Infant, Newborn
Infant, Premature
Intestinal Diseases
Male
Mutation, Missense
Phenotype
Polyendocrinopathies, Autoimmune
Syndrome
T-Lymphocytes, Regulatory
| | Language | eng | | Pub Type(s) | Case Reports
Letter
Research Support, Non-U.S. Gov't
| | PubMed ID | 19846862 |
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