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Transcobalamin deficiency - a rare genetic defect in transportation of cobalamin; case report.
Case report: Novel compound-heterozygous mutations in the TCN2 gene identified in a chinese girl with transcobalamin deficiency.
A novel TCN2 mutation with unusual clinical manifestations of hemolytic crisis and unexplained metabolic acidosis: expanding the genotype and phenotype of transcobalamin II deficiency.
Subclinical maculopathy and retinopathy in transcobalamin deficiency: a 10-year follow-up.
Spectroscopic and computational insight into the conformational dynamics of hemoglobin in the presence of vitamin B12.