NFKB2 Mutation Diagnosed by Whole Exome Sequencing (WES) in a Patient with Complex Phenotype and Hypogammaglobulinemia

Abstrakt

Poster presents NFKB2 Mutation Diagnosed by Whole Exome Sequencing (WES) in a Patient with Complex Phenotype and Hypogammaglobulinemia

Klíčová slova

• NFKB2
• Exome Sequencing
• WES
• Complex Phenotype
• Hypogammaglobulinemia