Disruption of hSWI/SNF complexes in T cells by WAS mutations distinguishes X-linked thrombocytopenia from Wiskott-Aldrich syndrome. [electronic resource]
Producer: 20150223Description: 3409-19 p. digitalISSN:- 1528-0020
- Cell Nucleus -- genetics
- Cells, Cultured
- Chromosomal Proteins, Non-Histone -- genetics
- Diagnosis, Differential
- Genetic Diseases, X-Linked -- diagnosis
- Humans
- Mutation
- Promoter Regions, Genetic
- T-Lymphocytes -- metabolism
- Th1 Cells -- metabolism
- Thrombocytopenia -- diagnosis
- Transcription Factors -- genetics
- Wiskott-Aldrich Syndrome -- diagnosis
- Wiskott-Aldrich Syndrome Protein -- genetics
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Publication Type: Journal Article; Research Support, N.I.H., Extramural
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