Deletion of chr7p22 and chr15q11: Two Familial Cases of Immune Deficiency: Extending the Phenotype Toward Dysimmunity

Conclusion: We discuss here how the PDGFa, CARD11, LFNG, GPER1 and MAFK genes, included in the deletion 7p22, could be involved in the clinical and biological features of the two patients.
Source: Frontiers in Immunology - Category: Allergy & Immunology Source Type: research