Severe combined immunodeficiency with a homozygous c.464T>C (p.Leu155Pro) mutation in the RAG2 gene in a country without neonatal screening: Report of two clinical cases
Crossref DOI link: https://doi.org/10.53022/oarjbp.2023.9.1.0046
Published Online: 2023-10-30
Update policy: https://doi.org/10.53022/oarj.ourcrossmarkpolicy
Zurisadai Raquel García Osorno,
Augusto Ignacio Siegert Olivares,
Paola Alejandra Cisneros Conklin,
Ibeth Judith Reyes Montante,
María Andrea Murillo Gallo,
