Predominant antibody deficiencies: in search of causes for clinical phenotypes and etiological diversity

Nartiša, Inga (Project leader)
Kurjāne, Nataļja (Supervisor)

Department of Biology and Microbiology

1 Meeting Abstract

1 results
- Publication Year, Title(ascending)
- Title

2024
Unusual presentation of DCLRE1C gene-related SCID: A case report of challenging molecular diagnosis
Rozevska, M., Armite, V., Taurina, G., Grantiņa, I., Nartiša, I., Rots, D. & Kurjāne, N., 2024, In: European Journal of Human Genetics. 32, Suppl. 2, p. 1041 - 1041 1 p., EP09.031.
Research output: Contribution to journal › Meeting Abstract › peer-review

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