
Keywords: فولیکولین; Smith-Magenis syndrome; Chromosome 17p11.2 deletion; Immune deficiency; Autoantibody; TNFRSF13B; FLCN; TOM1L2; B-cell tolerance; BHDS; Birt-Hogg-Dubé syndrome; CVID; Common variable immune deficiency; EMR; Electronic medical records; FLCN; Folliculin; Hi