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Omenn Syndrome Associated with a Functional Reversion Due to a Somatic Second-Site Mutation in CARD11 Deficiency

Document Type

ConferencePaper

Author

Fuchs, S; Rensing-Ehl, A; Pannicke, U; Lorenz, M; Jeelall, Y; Rohr, J; Speckmann, C; Vraetz, T; Farmand, S; Schmitt-Graeff, A; Fisch, P; Strahm, B; Henneke, P; Enders, A; Horikawa, K; Goodnow, C; Schwarz, K; Ehl, S

Source

JOURNAL OF CLINICAL IMMUNOLOGY. 34:S474-S475

Subject

Medicin och hälsovetenskap

Language

English
English

ISSN

0271-9142

Online Access

Full Text (ProQuest Central) Full Text (Springer-Archive) Web of Science JCR 저널정보 Find it@PNU

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