Prevalence of mutations in ELANE, GFI1, HAX1, SBDS, WAS and G6PC3 in patients with severe congenital neutropenia. [electronic resource]
Producer: 20100330Description: 535-42 p. digitalISSN:- 1365-2141
- Adaptor Proteins, Signal Transducing
- Chronic Disease
- DNA Mutational Analysis -- methods
- DNA-Binding Proteins -- genetics
- Female
- Genetic Predisposition to Disease
- Genotype
- Glucose-6-Phosphatase -- genetics
- Humans
- Leukocyte Elastase -- genetics
- Male
- Mutation
- Neutropenia -- congenital
- Proteins -- genetics
- Transcription Factors -- genetics
- Wiskott-Aldrich Syndrome Protein -- genetics
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Publication Type: Journal Article; Research Support, N.I.H., Extramural; Research Support, Non-U.S. Gov't
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