Extreme Phenotypes With Identical Mutations: Two Patients With Same Non-sense NHEJ1 Homozygous Mutation

María J. Recio1,2, Nerea Domínguez‐Pinilla2,3, Melina Soledad Perrig1,2, Carmen Rodriguez Vigil-Iturrate4, Nerea Salmón-Rodriguez5,2,6, Cristina Martínez Faci4, María José Castro-Panete7, Javier Blas-Espada7,2, Marta López-Nevado7,2, Raquel Ruiz‐García7,2, Rebeca Chaparro-García1, Luís M. Allende7,2, Luis Ignacio González‐Granado5,2,6
1Department of Immunology, Ophthalmology and ENT, School of Medicine, Complutense University, 12 de Octubre Health Research Institute (imas12), Madrid, Spain
2Hospital 12 de Octubre Health Research Institute (imas12), Madrid, Spain
3Pediatric Hematology and Oncology Unit, University Hospital Virgen de la Salud, Toledo, Spain
4Pediatric Hematology and Oncology Unit, University Hospital Miguel Servet, Zaragoza, Spain
5Complutense University School of Medicine, Madrid, Spain
6Immunodeficiencies Unit, Pediatrics, University Hospital 12 octubre, Madrid, Spain
7Department of Immunology, University Hospital 12 Octubre, Madrid, Spain

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