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1.
Heterozygous activating mutation in RAC2 causes infantile-onset combined immunodeficiency with susceptibility to viral infections.
Clin Immunol
; 205: 1-5, 2019 08.
Artículo
en Inglés
| MEDLINE | ID: mdl-31071452
2.
The Clinical and Genetic Spectrum of 82 Patients With RAG Deficiency Including a c.256_257delAA Founder Variant in Slavic Countries.
Front Immunol
; 11: 900, 2020.
Artículo
en Inglés
| MEDLINE | ID: mdl-32655540
3.
Geographical Distribution, Incidence, Malignancies, and Outcome of 136 Eastern Slavic Patients With Nijmegen Breakage Syndrome and NBN Founder Variant c.657_661del5.
Front Immunol
; 11: 602482, 2020.
Artículo
en Inglés
| MEDLINE | ID: mdl-33488600
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