. . . . . . . . . . . . "[All three new mutations alter amino acids in heptad repeats within the third coiled-coil region of the KIF21A stalk, highlighting the importance of alterations in this domain in the etiology of Congenital fibrosis of the extraocular muscles types 1 and 3.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine."@en . . . . . "2009-03-31"^^ . . "Gene-disease associations inferred from text-mining the literature."@en . "DisGeNET evidence - LITERATURE"@en . "2014-10-02T12:33:11+02:00"^^ . . . . . . . . . . . "v2.1.0.0" . "v2.1.0" .