Matches in Nanopublications for { ?s ?p "[Mutations in the KCNQ4 K+ channel gene, responsible for autosomal dominant hearing loss, cluster in the channel pore region.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine."@en ?g. }
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- NP3486.RAZtaY8tBSJnIw3V3g59e9VvMQ_yucIpmYo_TlmXWXTbs130_assertion description "[Mutations in the KCNQ4 K+ channel gene, responsible for autosomal dominant hearing loss, cluster in the channel pore region.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP3486.RAZtaY8tBSJnIw3V3g59e9VvMQ_yucIpmYo_TlmXWXTbs130_provenance.
- NP3021.RAFcxCNpWcfMoqZdAz7_o9-3H1vD3TutOCbicR6sUJ26c130_assertion description "[Mutations in the KCNQ4 K+ channel gene, responsible for autosomal dominant hearing loss, cluster in the channel pore region.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP3021.RAFcxCNpWcfMoqZdAz7_o9-3H1vD3TutOCbicR6sUJ26c130_provenance.
- assertion description "[Mutations in the KCNQ4 K+ channel gene, responsible for autosomal dominant hearing loss, cluster in the channel pore region.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." provenance.
- NP936.RAPA6ZLzhRot6fK7vGNDxbsyNnxmbBrqagmo5NowGOW-o130_assertion description "[Mutations in the KCNQ4 K+ channel gene, responsible for autosomal dominant hearing loss, cluster in the channel pore region.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP936.RAPA6ZLzhRot6fK7vGNDxbsyNnxmbBrqagmo5NowGOW-o130_provenance.