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Omenn Syndrome Associated with a Functional Reversion Due to a Somatic Second-Site Mutation in CARD11 Deficiency
- Fuchs, S (author)
- Rensing-Ehl, A (author)
- Pannicke, U (author)
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- Lorenz, M (author)
- Jeelall, Y (author)
- Rohr, J (author)
- Speckmann, C (author)
- Vraetz, T (author)
- Farmand, S (author)
- Schmitt-Graeff, A (author)
- Fisch, P (author)
- Strahm, B (author)
- Henneke, P (author)
- Enders, A (author)
- Horikawa, K (author)
- Goodnow, C (author)
- Schwarz, K (author)
- Ehl, S (author)
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- 2014
- 2014
- English.
- In: JOURNAL OF CLINICAL IMMUNOLOGY. - 0271-9142. ; 34, s. S474-S475
- Conference paper (other academic/artistic)
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- kon (subject category)
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- Fuchs, S
- Rensing-Ehl, A
- Pannicke, U
- Lorenz, M
- Jeelall, Y
- Rohr, J
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- Speckmann, C
- Vraetz, T
- Farmand, S
- Schmitt-Graeff, ...
- Fisch, P
- Strahm, B
- Henneke, P
- Enders, A
- Horikawa, K
- Goodnow, C
- Schwarz, K
- Ehl, S
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- JOURNAL OF CLINI ...
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- Karolinska Institutet
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