Mendonça, Leonardo Oliveira; Grassi, A; Cordova, Pablo Michael Torres; Amorim, L C; Castro, Fabio Fernandes Morato; Pontillo, Alessandra 
; Ceccherini, I; Gattorno, M; Barros, Myrthes Anna Maragna Toledo
Source: Journal of Clinical Immunology. Conference titles: 2017 LASID Meeting Abstracts. Unidades: FM, ICB
Subjects: IMUNOLOGIA, MUTAÇÃO, OSTEOMIELITE, GENÔMICA
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MENDONÇA, Leonardo Oliveira et al. A Case Report of a Novel Compound Heterozygous Mutation in a Brazilian Patient with Deficiency of IL1RA (DIRA). Journal of Clinical Immunology. New York: Springer New York LLC. Disponível em: https://doi.org/10.1007/s10875-017-0442-2. Acesso em: 31 out. 2024. , 2017APA
Mendonça, L. O., Grassi, A., Cordova, P. M. T., Amorim, L. C., Castro, F. F. M., Pontillo, A., et al. (2017). A Case Report of a Novel Compound Heterozygous Mutation in a Brazilian Patient with Deficiency of IL1RA (DIRA). Journal of Clinical Immunology. New York: Springer New York LLC. doi:10.1007/s10875-017-0442-2NLM
Mendonça LO, Grassi A, Cordova PMT, Amorim LC, Castro FFM, Pontillo A, Ceccherini I, Gattorno M, Barros MAMT. A Case Report of a Novel Compound Heterozygous Mutation in a Brazilian Patient with Deficiency of IL1RA (DIRA) [Internet]. Journal of Clinical Immunology. 2017 ; 37 S19.[citado 2024 out. 31 ] Available from: https://doi.org/10.1007/s10875-017-0442-2Vancouver
Mendonça LO, Grassi A, Cordova PMT, Amorim LC, Castro FFM, Pontillo A, Ceccherini I, Gattorno M, Barros MAMT. A Case Report of a Novel Compound Heterozygous Mutation in a Brazilian Patient with Deficiency of IL1RA (DIRA) [Internet]. Journal of Clinical Immunology. 2017 ; 37 S19.[citado 2024 out. 31 ] Available from: https://doi.org/10.1007/s10875-017-0442-2
