Matches in Nanopublications for { ?s ?p "[Several different mutations in the KCNQ4 K+ channel gene are responsible for autosomal dominant nonsyndromic hearing impairment (DFNA2).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine."@en ?g. }
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- NP815722.RAVMvlafz-VSO9uXgKYknUlsAX7ia6waApyWXmcAUhbIc130_assertion description "[Several different mutations in the KCNQ4 K+ channel gene are responsible for autosomal dominant nonsyndromic hearing impairment (DFNA2).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP815722.RAVMvlafz-VSO9uXgKYknUlsAX7ia6waApyWXmcAUhbIc130_provenance.
- assertion description "[Several different mutations in the KCNQ4 K+ channel gene are responsible for autosomal dominant nonsyndromic hearing impairment (DFNA2).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." provenance.
- NP360531.RAz7aGL-paETX7ZSiHOojNF6yy3UB46CPwijfJZEz3G2M130_assertion description "[Several different mutations in the KCNQ4 K+ channel gene are responsible for autosomal dominant nonsyndromic hearing impairment (DFNA2).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP360531.RAz7aGL-paETX7ZSiHOojNF6yy3UB46CPwijfJZEz3G2M130_provenance.