Matches in Nanopublications for { ?s ?p "[In families with recessively inherited deafness, DFNB37, our sequence analyses of MYO6 reveal a frameshift mutation (36-37insT), a nonsense mutation (R1166X), and a missense mutation (E216V).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine."@en ?g. }
Showing items 1 to 1 of
1
with 100 items per page.
- NP894180.RAmZyIMCsb87dfbb62sPuTn3pL4ldDi6tTM0Kmzs8gNT8130_assertion description "[In families with recessively inherited deafness, DFNB37, our sequence analyses of MYO6 reveal a frameshift mutation (36-37insT), a nonsense mutation (R1166X), and a missense mutation (E216V).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP894180.RAmZyIMCsb87dfbb62sPuTn3pL4ldDi6tTM0Kmzs8gNT8130_provenance.