Omenn syndrome associated with a functional reversion due to a somatic second-site mutation in CARD11 deficiency

Citation

Fuchs S, Rensing-Ehl A, Pannicke U, Lorenz MR, Fisch P, Jeelall Y, Rohr J, Speckmann C, Vraetz T, Farmand S, Schmitt-Graeff A, Krüger M, Strahm B, Henneke P, Enders A, Horikawa K, Goodnow C, Schwarz K, Ehl S. 2015, 'Omenn syndrome associated with a functional reversion due to a somatic second-site mutation in CARD11 deficiency', Blood, vol. 126, no. 14, pp. 1658-1669.

Year

2015

ANU Authors

Field of Research

  • Oncology And Carcinogenesis Not Elsewhere Classified

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