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Fig. 4 | Orphanet Journal of Rare Diseases

Fig. 4

From: Identification and in silico analysis of a spectrum of SLC4A11 variations in Indian familial and sporadic cases of congenital hereditary endothelial dystrophy

Fig. 4

SLC4A11 mutational effects on the number of hydrogen bond interactions around the 5 Å region of the mutation. A1, B1, and C1 shows the number of H bonds of WT SLC4A11 at S489, R869, and S480 positions, respectively. A2, B2, and C2 shows the corresponding number of H bonds after it mutates to W489, C869, and I480, respectively

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Orphanet Journal of Rare Diseases

ISSN: 1750-1172