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

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Bibliographic Details
Main Authors: 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
Format: Conference Proceeding
Language:English
Subjects:
Medicin och hälsovetenskap
Online Access:Get full text
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ISSN:0271-9142