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Publikováno v:
BMJ Case Reports
Severe combined immunodeficiency (SCID) is an extremely rare disease caused by a disruption in the forkhead box N1 (FOXN1) gene, with an incidence of FOXN1 gene. The variant was confirmed with Sanger sequencing. Management of EBV infection and lympho
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::9ae7fbe4f63e8c2ac8d9fa88fcd56f9f
https://pubmed.ncbi.nlm.nih.gov/31151968
https://pubmed.ncbi.nlm.nih.gov/31151968
