Compound heterozygosity for one novel and one recurrent mutation in a Thai patient with severe protein S deficiency

بواسطة Parichat Pung-Amritt, Swibertus R. Poort, Hans L. Vos, Rogier M. Bertina, Chularatana Mahasandana, Voravarn S. Tanphaichitr, Gavivann Veerakul, Suthida Kankirawatana, Vinai Suvatte
منشور في 2018