A novel GJA8 mutation is associated with autosomal dominant lamellar pulverulent cataract: further evidence for gap junction dysfunction in human cataract.
- Cited forVARIANT CTRCT1 GLN-88, CHARACTERIZATION OF VARIANT CTRCT1 GLN-88, SUBCELLULAR LOCATION, FUNCTION
- CategoriesFunction, Sequences, Subcellular Location
- SourceUniProtKB reviewed (Swiss-Prot)