Matches in Nanopublications for { ?s ?p "[A novel missense mutation in ACTG1 causes dominant deafness in a Norwegian DFNA20/26 family, but ACTG1 mutations are not frequent among families with hereditary hearing impairment.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine."@en ?g. }
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- assertion description "[A novel missense mutation in ACTG1 causes dominant deafness in a Norwegian DFNA20/26 family, but ACTG1 mutations are not frequent among families with hereditary hearing impairment.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." provenance.
- NP171.RAcbDqzNoH-eu0VA6lZ0XvNqmI7GhcFmULSbP-jWQjDzA130_assertion description "[A novel missense mutation in ACTG1 causes dominant deafness in a Norwegian DFNA20/26 family, but ACTG1 mutations are not frequent among families with hereditary hearing impairment.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP171.RAcbDqzNoH-eu0VA6lZ0XvNqmI7GhcFmULSbP-jWQjDzA130_provenance.
- NP4559.RA49yrW2D59Qy3J-i9-JXaVpy_uLW-gYFuKyqG_tW2DT0130_assertion description "[A novel missense mutation in ACTG1 causes dominant deafness in a Norwegian DFNA20/26 family, but ACTG1 mutations are not frequent among families with hereditary hearing impairment.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP4559.RA49yrW2D59Qy3J-i9-JXaVpy_uLW-gYFuKyqG_tW2DT0130_provenance.