| Literature DB >> 30466769 |
Abstract
Since the first genes associated with primary immunodeficiency were described in the early 1990s, there has been an exponential increase the number of genes found to have pathologic variants in patients with symptoms of primary immunodeficiency. Genetic testing currently used clinically includes chromosomal microarray, Sanger sequencing, and next-generation sequencing techniques, including whole exome testing. With the knowledge of the underlying molecular pathways, biologic therapies have been used for treatment and efforts are underway to broaden the availability of gene therapy.Entities:
Keywords: Chromosomal microarray; Gene editing; Gene therapy; Next-generation sequencing; Primary immunodeficiency; Sanger sequencing; Whole exome sequencing; Whole genome sequencing
Mesh:
Year: 2019 PMID: 30466769 DOI: 10.1016/j.iac.2018.08.009
Source DB: PubMed Journal: Immunol Allergy Clin North Am ISSN: 0889-8561 Impact factor: 3.479