Asian-specific mtDNA backgrounds associated with the primary G11778A mutation of Leber's hereditary optic neuropathy

بواسطة Herawati Sudoyo, Helena Suryadi, Patcharee Lertrit, Patcharin Pramoonjago, Diana Lyrawati, Sangkot Marzuki
منشور في 2018

Genotypic and phenotypic implications in paroxysmal nocturnal hemoglobinuria (PNH): A preliminary investigation

بواسطة Kriangsak Pakdeesuwan, Uamporn Siripanyaphinyo, Patcharin Pramoonjago, Kovit Pattanapanyasat, Prapon Wilairat, Taroh Kinoshita, Wanchai Wanachiwanawin
منشور في 2018