A novel TCN2 mutation with unusual clinical manifestations of hemolytic crisis and unexplained metabolic acidosis: expanding the genotype and phenotype of transcobalamin II deficie...

by Khongkraparn, A., Pongphitcha, P., Sirachainan, N., Songdej, D., Tim-Aroon, T., Wattanasirichaigoon, D.
Published 2022