Disruption of hSWI/SNF complexes in T cells by WAS mutations distinguishes X-linked thrombocytopenia from Wiskott-Aldrich syndrome.

Sarkar, Koustav

Disruption of hSWI/SNF complexes in T cells by WAS mutations distinguishes X-linked thrombocytopenia from Wiskott-Aldrich syndrome. [electronic resource] - Blood Nov 2014 - 3409-19 p. digital

Publication Type: Journal Article; Research Support, N.I.H., Extramural

1528-0020

10.1182/blood-2014-07-587642 doi


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