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Fig. 1 | BMC Pediatrics

Fig. 1

From: Analysis of the relationship between the mutation site of the SLC39A4 gene and acrodermatitis enteropathica by reporting a rare Chinese twin: a case report and review of the literature

Fig. 1

Pedigrees of the families. Icons corresponding to the individuals we examined are marked. People exhibiting a mutation in both alleles of SLC39A4 are identified by symbols filled in black. Heterozygote carriers for a unique mutation are symbolized by half-filled icons. By default, all the untested people, including some parents, are represented by white icons

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BMC Pediatrics

ISSN: 1471-2431

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