Congenital endothelial dystrophy type 2
Encyclopedia
Congenital endothelial dystrophy type 2 is a rare form of human corneal dystrophy. It is associated with mutations in SLC4A11
SLC4A11
Sodium bicarbonate transporter-like protein 11 is a protein that in humans is encoded by the SLC4A11 gene.-Further reading:...

 gene.

See also

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