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. 2021 Jul 1;12:683255. doi: 10.3389/fgene.2021.683255

FIGURE 4.

FIGURE 4

The schematic of SLC19A3 protein and the location of all identified mutations. Mutations in light blue were discovered in patients with classical BTBGD. Mutations in dark blue were found in patients with infantile phenotypes. Mutations in yellow box were found in both classical and infantile phenotypes. Mutations in black box were found in Wernicke’s-like encephalopathy.