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1.
A large deletion in a non-coding regulatory region leads to NFKB1 haploinsufficiency in two adult siblings.
Clin Immunol
; 261: 110165, 2024 04.
Article
in English
| MEDLINE | ID: mdl-38423196
2.
Compound heterozygous mutations in the kinase domain of IKKα lead to immunodeficiency and immune dysregulation.
medRxiv
; 2024 May 17.
Article
in English
| MEDLINE | ID: mdl-38798321
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