Cargando…
Severe combined immunodeficiency syndrome with RAG1 mutation gene - case report
Autores principales: | Lima, Ana Lúcia, Andrade, Hevila, Sundin, Erika, Loureiro, Patricia, Gonçalves, Juliana, Guirau, Lúcia, Umeta, Aline, Pereira, Vanessa, Cohon, Andrea |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
World Allergy Organization
2015
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4406427/ http://dx.doi.org/10.1186/1939-4551-8-S1-A178 |
Ejemplares similares
-
The R229Q mutation of Rag2 does not characterize severe immunodeficiency in mice
por: Jin, Young, et al.
Publicado: (2019) -
Severe combined immunodeficiency: case report of alogenic, haploidentical bone marrow transplantation
por: Silveira, Fernanda, et al.
Publicado: (2015) -
Expression of RAG1, RAG2, and TdT in Rheumatoid Arthritis Synovia: Evidence for Receptor Revision of Immunoglobulin Light Chains
por: Bridges Jr, S Louis, et al.
Publicado: (2000) -
Partial correction of immunodeficiency by lentiviral vector gene therapy in mouse models carrying Rag1 hypomorphic mutations
por: Castiello, Maria Carmina, et al.
Publicado: (2023) -
A variant of RAG1 gene identified in severe combined immunodeficiency: a case report
por: Zhang, Xinping, et al.
Publicado: (2023)