학술논문
DCLRE1C (ARTEMIS) mutations causing phenotypes ranging from atypical severe combined immunodeficiency to mere antibody deficiency
Document Type
Artikel
Author
Volk, T; Pannicke, U; Reisli, I; Bulashevska, A; Ritter, J; Bjorkman, A; Schaffer, AA; Fliegauf, M; Sayar, EH; Salzer, U; Fisch, P; Pfeifer, D; Di Virgilio, M; Cao, HZ; Yang, F; Zimmermann, K; Keles, S; Caliskaner, Z; Guner, S; Schindler, D; Hammarstrom, L; Rizzi, M; Hummel, M; Pan-Hammarstrom, Q; Schwarz, K; Grimbacher, B
Source
Human molecular genetics. 24(25):7361-7372
Subject
Language
English
English
English
ISSN
1460-2083