Novel ZBTB24 Mutation Associated with Immunodeficiency, Centromere Instability, and Facial Anomalies Type-2 Syndrome Identified in a Patient with Very Early Onset Inflammatory Bowel Disease.

Conrad MA, Dawany N, Sullivan KE, Devoto M, Kelsen JR. Novel ZBTB24 Mutation Associated with Immunodeficiency, Centromere Instability, and Facial Anomalies Type-2 Syndrome Identified in a Patient with Very Early Onset Inflammatory Bowel Disease. Inflamm Bowel Dis. 2017 12; 23(12):2252-2255.

View in: PubMed

subject areas

Centromere
Duodenum
Face
Humans
Immunologic Deficiency Syndromes
Infant
Inflammatory Bowel Diseases
Male
Mutation
Repressor Proteins

authors with profiles

Kathleen Sullivan, APRN, PMHCNS-BC

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