Matches in Nanopublications for { ?s ?p "[The results demonstrate that KIF21A mutations are a rare cause of CFEOM3 (congenital fibrosis of the extraocular muscles) ]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine."@en ?g. }
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- NP137584.RAAWozGPFal8dZlXcxuUTraPaDWCZICvZ36D1Eugwta-U130_assertion description "[The results demonstrate that KIF21A mutations are a rare cause of CFEOM3 (congenital fibrosis of the extraocular muscles) ]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP137584.RAAWozGPFal8dZlXcxuUTraPaDWCZICvZ36D1Eugwta-U130_provenance.
- NP200734.RAhVlQXg1hknLbuzmOwTyHHHC5Zx124-Rf3pX6WbSNQeI130_assertion description "[The results demonstrate that KIF21A mutations are a rare cause of CFEOM3 (congenital fibrosis of the extraocular muscles) ]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP200734.RAhVlQXg1hknLbuzmOwTyHHHC5Zx124-Rf3pX6WbSNQeI130_provenance.
- NP205724.RA5Kwjo9RmfY5dicVyl4oZSZxonbLerEjNyTNxDZQ9utU130_assertion description "[The results demonstrate that KIF21A mutations are a rare cause of CFEOM3 (congenital fibrosis of the extraocular muscles) ]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP205724.RA5Kwjo9RmfY5dicVyl4oZSZxonbLerEjNyTNxDZQ9utU130_provenance.