Matches in Nanopublications for { ?s ?p "[A novel dominant missense mutation--D179N--in the GJB2 gene (Connexin 26) associated with non-syndromic hearing loss.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine."@en ?g. }
Showing items 1 to 5 of
5
with 100 items per page.
- NP2733.RAY7uu5aAR_3_wCWIwrTSiPI_-_n-BDCJ4AiWmcBJpb0g130_assertion description "[A novel dominant missense mutation--D179N--in the GJB2 gene (Connexin 26) associated with non-syndromic hearing loss.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP2733.RAY7uu5aAR_3_wCWIwrTSiPI_-_n-BDCJ4AiWmcBJpb0g130_provenance.
- assertion description "[A novel dominant missense mutation--D179N--in the GJB2 gene (Connexin 26) associated with non-syndromic hearing loss.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." provenance.
- assertion description "[A novel dominant missense mutation--D179N--in the GJB2 gene (Connexin 26) associated with non-syndromic hearing loss.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." provenance.
- NP2710.RAXlpdvIsyOVBdTlDu8oK-1HiIuSTKCJdwaBirL1rQF1Q130_assertion description "[A novel dominant missense mutation--D179N--in the GJB2 gene (Connexin 26) associated with non-syndromic hearing loss.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP2710.RAXlpdvIsyOVBdTlDu8oK-1HiIuSTKCJdwaBirL1rQF1Q130_provenance.
- NP396803.RAeuNZoz2GaIapfkGi-mk3_Fen9h3ELtnoQyZcKeFTlY8130_assertion description "[A novel dominant missense mutation--D179N--in the GJB2 gene (Connexin 26) associated with non-syndromic hearing loss.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP396803.RAeuNZoz2GaIapfkGi-mk3_Fen9h3ELtnoQyZcKeFTlY8130_provenance.