A POINT MUTATION CREATING A 3′ SPLICE SITE IN C8A IS A PREDOMINANT CAUSE OF C8α-γ DEFICIENCY IN AFRICAN AMERICANS

Autor Densen, Peter, Ackermann, Laynez, Saucedo, Leslie, Figueroa, Julio E., Si, Zhi-hai, Stoltzfus, Conrad Martin
Vydáno v J Immunol (2020)