4.0 Letter

Fuchs Endothelial Corneal Dystrophy in a Heterozygous Carrier of Congenital Hereditary Endothelial Dystrophy Type 2 with a Novel Mutation in SLC4A11

Related references

Note: Only part of the references are listed.
Article Biochemistry & Molecular Biology

A Biochemical Framework for SLC4A11, the Plasma Membrane Protein Defective in Corneal Dystrophies

Gonzalo L. Vilas et al.

BIOCHEMISTRY (2011)

Article Biochemistry & Molecular Biology

SLC4A11 mutations in Fuchs endothelial corneal dystrophy

Eranga N. Vithana et al.

HUMAN MOLECULAR GENETICS (2008)

Article Genetics & Heredity

Autosomal recessive corneal endothelial dystrophy (CHED2) is associated with mutations in SLC4A11

Xiaodong Jiao et al.

JOURNAL OF MEDICAL GENETICS (2007)