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A major mutation of KIF21A associated with congenital fibrosis of the extraocular muscles type 1 (CFEOM1) enhances translocation of Kank1 to the membrane

Extraocular MusclesCongenital FibrosisFibrosisMolecular PhysiologyDevelopmental BiologyGenetic DisorderGeneticsMajor MutationMedicineCell BiologyCellular PhysiologyConnective Tissue Disease