Matches in Nanopublications for { ?s ?p "[Here, we show that mutations in the inwardly rectifying K(+) channel gene KCNJ10 are associated with nonsyndromic hearing loss in carriers of SLC26A4 mutations with an EVA/PS phenotype.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine."@en ?g. }
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- NP920620.RAhnkQt-H4112zTRZeh0njmn8Rvc5sjq0QwXXCZGN-OPE130_assertion description "[Here, we show that mutations in the inwardly rectifying K(+) channel gene KCNJ10 are associated with nonsyndromic hearing loss in carriers of SLC26A4 mutations with an EVA/PS phenotype.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP920620.RAhnkQt-H4112zTRZeh0njmn8Rvc5sjq0QwXXCZGN-OPE130_provenance.
- NP296779.RA3iNGJxAmy5FTPBGODypg1MzUCxmTZ9cBHHh7Ze6YMEM130_assertion description "[Here, we show that mutations in the inwardly rectifying K(+) channel gene KCNJ10 are associated with nonsyndromic hearing loss in carriers of SLC26A4 mutations with an EVA/PS phenotype.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP296779.RA3iNGJxAmy5FTPBGODypg1MzUCxmTZ9cBHHh7Ze6YMEM130_provenance.
- NP763252.RAxtZOo8_JrsXj7TBRvN4MSrBW6hgyLvC3VJKPkJewSGk130_assertion description "[Here, we show that mutations in the inwardly rectifying K(+) channel gene KCNJ10 are associated with nonsyndromic hearing loss in carriers of SLC26A4 mutations with an EVA/PS phenotype.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP763252.RAxtZOo8_JrsXj7TBRvN4MSrBW6hgyLvC3VJKPkJewSGk130_provenance.
- assertion description "[Here, we show that mutations in the inwardly rectifying K(+) channel gene KCNJ10 are associated with nonsyndromic hearing loss in carriers of SLC26A4 mutations with an EVA/PS phenotype.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." provenance.
- NP737514.RA-OVaw3UO1MoA1emTGUpaNumO59UWMJIZvD_DRTXnJwU130_assertion description "[Here, we show that mutations in the inwardly rectifying K(+) channel gene KCNJ10 are associated with nonsyndromic hearing loss in carriers of SLC26A4 mutations with an EVA/PS phenotype.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP737514.RA-OVaw3UO1MoA1emTGUpaNumO59UWMJIZvD_DRTXnJwU130_provenance.