HSCT in a Patient with Cernunnos/XLF Deficiency and Omenn Syndrome

J Clin Immunol. 2024 Sep 12;45(1):5. doi: 10.1007/s10875-024-01765-y.

Marwa Chbihi^{1

2}, Léa Nabhan³, Antoine Pinton⁴, Philippe Drabent⁵, Jean-Pierre de Villartay³, Bénédicte Neven^{6

7

8}

¹ Pediatric Immunology-Hematology and Rheumatology Unit, Necker Hospital for Sick Children, AP-HP, 149 Rue de Sèvres, 75015, Paris, France.
² Paris-Cité University, Paris, France.
³ Laboratory of Genome Dynamics in the Immune System, INSERM UMR 1163, Imagine Institute, Paris, France.
⁴ Institut Necker Enfants Malades, UMR 1151, INSERM, Paris, France.
⁵ Department of Pathology, Necker Hospital for Sick Children, AP-HP, Paris, France.
⁶ Pediatric Immunology-Hematology and Rheumatology Unit, Necker Hospital for Sick Children, AP-HP, 149 Rue de Sèvres, 75015, Paris, France. [email protected].
⁷ Paris-Cité University, Paris, France. [email protected].
⁸ Laboratory of Immunogenetics of Pediatric Autoimmune Diseases, INSERM UMR 1163, Imagine Institute, Paris, France. [email protected].

No abstract available

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