Major histocompatibility complex class II expression deficiency caused by a RFXANK founder mutation: a survey of 35 patients

Partial recessive IFN-γR1 deficiency: genetic, immunological and clinical features of 14 patients from 11 kindreds

(2011) Ithaisa Sologuren et al.   HUMAN MOLECULAR GENETICS

Allogeneic Stem Cell Transplantation Using Myeloablative and Reduced-Intensity Conditioning in Patients with Major Histocompatibility Complex Class II Deficiency

(2010) Hamoud Al-Mousa et al.   BIOLOGY OF BLOOD AND MARROW TRANSPLANTATION

The 752delG26 mutation in the RFXANK gene associated with major histocompatibility complex class II deficiency: evidence for a founder effect in the Moroccan population

(2010) Hamid Naamane et al.   EUROPEAN JOURNAL OF PEDIATRICS

Two Newly Diagnosed HLA Class II-Deficient Patients Identified by Rapid Vector-Based Complementation Analysis Reveal Discoordinate Invariant Chain Expression Levels

(2010) Klaus G. Schmetterer et al.   INTERNATIONAL ARCHIVES OF ALLERGY AND IMMUNOLOGY

MHC class II deficiency cured by unrelated mismatched umbilical cord blood transplantation: Case report and review of 68 cases in the literature

(2010) M. Siepermann et al.   PEDIATRIC TRANSPLANTATION

MHC class 2 deficiency and X-linked agammaglobulinaemia in a consanguineous extended family

(2009) A. Broides et al.   International Journal of Immunogenetics

Unrelated cord blood transplantation and reduced-intensity conditioning regimen for graft failure in a child with Major Histocompatibility Complex class II deficiency

(2008) M Bonduel et al.   BONE MARROW TRANSPLANTATION

Primary Immunodeficiency Disorders: Survey of Pediatricians in Kuwait

(2008) Waleed Al-Herz et al.   JOURNAL OF CLINICAL IMMUNOLOGY

Primary Immunodeficiency Diseases in Egyptian Children: A Single-Center Study

(2008) Shereen M. Reda et al.   JOURNAL OF CLINICAL IMMUNOLOGY