https://www.ncbi.nlm.nih.gov/Structure/pdb/5NRP
5NRP: Beta domain of human transcobalamin bound to cobinamide
Transcobalamin-2COB(II)INAMIDECYANIDE ION
betadomainhumanbound
https://pubmed.ncbi.nlm.nih.gov/14969589/
Methylenetetrahydrofolate reductase and transcobalamin genetic polymorphisms in human spontaneous...
The pathogenesis of human spontaneous abortion involves a complex interaction of several genetic and environmental factors. The firm association between...
in humanreductasegeneticspontaneous
https://pubmed.ncbi.nlm.nih.gov/20607612/
Transcobalamin deficiency caused by compound heterozygosity for two novel mutations in the TCN2...
Transcobalamin (TC) deficiency (OMIM# 275350) is a rare, autosomal recessive disorder that presents in early infancy with a broad spectrum of symptoms,...
https://medlineplus.gov/genetics/condition/transcobalamin-deficiency/
Transcobalamin deficiency: MedlinePlus Genetics
Transcobalamin deficiency is a disorder that impairs the transport of cobalamin (also known as vitamin B12) within the body. Explore symptoms, inheritance,...
deficiencymedlineplusgenetics