Associated Papers
Transcobalamin II Deficiency in an Infant with a Novel Mutation.
Toret E et al.
Turkish Archives of Pediatrics, 2022
Case report: Novel compound-heterozygous mutations in the TCN2 gene identified in a chinese girl with transcobalamin deficiency.
Luo J et al.
Frontiers in Genetics, 2022
Identification of transcobalamin deficiency with two novel mutations in the TCN2 gene in a Chinese girl with abnormal immunity: a case report.
Zhan S et al.
Bmc Pediatrics, 2020
Different Presentations of Patients with Transcobalamin II Deficiency: A Single-Center Experience from Turkey
Ünal S et al.
Turkish Journal of Haematology : Official Journal of Turkish Society of Haematology, 2019
Transcobalamin II Deficiency in Four Cases with Novel Mutations.
Ünal Ş et al.
Turkish Journal of Haematology : Official Journal of Turkish Society of Haematology, 2015
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