NUDCD3 deficiency disrupts V(D)J recombination to cause SCID and Omenn syndrome

Rui Chen, Elena Lukianova, Ina Schim van der Loeff, Jarmila Stremenova Spegarova, Joseph D.P. Willet, Kieran D James, Edward Ryder, Hanna IJspeert, Akshada Gajbhiye, Frederic Lamoliatte, José Luis Marín-Rubio, Lisa Woodbine, Henrique Lemos, David J. Swan, Valeria Pintar, Kamal Sayes, Elias Rafael Ruiz-Morales, Simon Eastham, David Dixon, Martin PreteElena Prigmore, Penny Jeggo, Joan Boyes, Andrew Mellor, lei huang, Mirjam van der Burg, Karin Regine Engelhardt, Asbjørg Stray-Pedersen, Hans Christian Erichsen, Andrew Gennery, Matthias Trost, graham anderson, Anna Lorenc, Gosia Trynka, Sophie Hambleton*

*Corresponding author for this work

Research output: Contribution to journalArticle (Academic Journal)peer-review

1 Citation (Scopus)

Fingerprint

Dive into the research topics of 'NUDCD3 deficiency disrupts V(D)J recombination to cause SCID and Omenn syndrome'. Together they form a unique fingerprint.

Immunology and Microbiology