1.
Clin Case Rep
; 9(4): 2023-2031, 2021 Apr.
Artículo
en Inglés
| MEDLINE
| ID: mdl-33936634
RESUMEN
We suggest PLAID, APLAID, and FCAS3 have to be considered as different aspects of the same underlying condition, because of our long-term clinical and genetical experiences. Some CVID patients have the same disease-causing mutations in PLCG2 gene, so it may be better to define all of them as "PLCG2deficiency."