ADA2 deficiency (DADA2) associated with Evans syndrome and a severe ADA2 genotype.
Publication
, Journal Article
Ferriani, MPL; Valera, ET; de Sousa, GR; Sandrin-Garcia, P; de Moura, RR; Hershfield, MS; de Carvalho, LM
Published in: Rheumatology (Oxford)
July 1, 2021
Duke Scholars
Published In
Rheumatology (Oxford)
DOI
EISSN
1462-0332
Publication Date
July 1, 2021
Volume
60
Issue
7
Start / End Page
e237 / e239
Location
England
Related Subject Headings
- Thrombocytopenia
- Severe Combined Immunodeficiency
- Sequence Deletion
- Pedigree
- Mutation, Missense
- Intercellular Signaling Peptides and Proteins
- Immunologic Factors
- Immunoglobulins, Intravenous
- Humans
- Glucocorticoids
Citation
APA
Chicago
ICMJE
MLA
NLM
Ferriani, M. P. L., Valera, E. T., de Sousa, G. R., Sandrin-Garcia, P., de Moura, R. R., Hershfield, M. S., & de Carvalho, L. M. (2021). ADA2 deficiency (DADA2) associated with Evans syndrome and a severe ADA2 genotype. Rheumatology (Oxford), 60(7), e237–e239. https://doi.org/10.1093/rheumatology/keab011
Ferriani, Mariana P. L., Elvis T. Valera, Graziella R. de Sousa, Paula Sandrin-Garcia, Ronald R. de Moura, Michel S. Hershfield, and Luciana M. de Carvalho. “ADA2 deficiency (DADA2) associated with Evans syndrome and a severe ADA2 genotype.” Rheumatology (Oxford) 60, no. 7 (July 1, 2021): e237–39. https://doi.org/10.1093/rheumatology/keab011.
Ferriani MPL, Valera ET, de Sousa GR, Sandrin-Garcia P, de Moura RR, Hershfield MS, et al. ADA2 deficiency (DADA2) associated with Evans syndrome and a severe ADA2 genotype. Rheumatology (Oxford). 2021 Jul 1;60(7):e237–9.
Ferriani, Mariana P. L., et al. “ADA2 deficiency (DADA2) associated with Evans syndrome and a severe ADA2 genotype.” Rheumatology (Oxford), vol. 60, no. 7, July 2021, pp. e237–39. Pubmed, doi:10.1093/rheumatology/keab011.
Ferriani MPL, Valera ET, de Sousa GR, Sandrin-Garcia P, de Moura RR, Hershfield MS, de Carvalho LM. ADA2 deficiency (DADA2) associated with Evans syndrome and a severe ADA2 genotype. Rheumatology (Oxford). 2021 Jul 1;60(7):e237–e239.
Published In
Rheumatology (Oxford)
DOI
EISSN
1462-0332
Publication Date
July 1, 2021
Volume
60
Issue
7
Start / End Page
e237 / e239
Location
England
Related Subject Headings
- Thrombocytopenia
- Severe Combined Immunodeficiency
- Sequence Deletion
- Pedigree
- Mutation, Missense
- Intercellular Signaling Peptides and Proteins
- Immunologic Factors
- Immunoglobulins, Intravenous
- Humans
- Glucocorticoids