A Novel Deletion in FERMT3 Causes LAD-III in a Turkish Family

In conclusion, beside the variant c.1525C > T in theFERMT3 gene, which was previously found in more than 15 patients in Anatolia, our study is the first to identify the novel homozygous variant c.921delC in theFERMT3 gene.

http://link.springer.com/10.1007/s10875-022-01420-4

Source: Journal of Clinical Immunology - January 17, 2023 Category: Allergy & Immunology Source Type: research