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Fig. 3 | BMC Pediatrics

Fig. 3

From: Identification of transcobalamin deficiency with two novel mutations in the TCN2 gene in a Chinese girl with abnormal immunity: a case report

Fig. 3

Protein structure prediction caused by compound heterozygous gene mutations of the TCN2 gene. a, The three-dimensional structure diagram of the wild-type TCN2 protein; the dashed box shows the C-terminal domain. b, The mutant of TCN2 p.Leu340Ter, the dashed box shows the lost C-terminal domain. c, The mutant of TCN2 p.Gln345Ter; the dashed box shows the lost C-terminal domain.

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BMC Pediatrics

ISSN: 1471-2431

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