A PRRT2 variant in a Chinese family with PKD/BFIS results in loss of interaction with STX1B
A PRRT2 variant in a Chinese family with PKD/BFIS results in loss of interaction with STX1B
复制标题
患有 PKD/BFIS 的中国家庭中的 PRRT2 变异导致与 STX1B 相互作用丧失
作者：
Ma H;Feng S;Deng X;Wang L;Zeng S;Wang C;Ma X;Sun H;Chen R;Du S;Mao J;Zhang X;Ma C;Jiang H;Zhang L;Tang B;Liu JY
