Matches in Nanopublications for { ?s ?p "[It is highly probable that mutations of connexin genes that result in human nonsyndromic deafness cause dysfunction of cochlear gap junctions and thereby interrupt K+ ion recirculation pathways.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine."@en ?g. }
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- NP343268.RATMXBHPLzcI5abrNsV207xFBC0DIu2N-n0xUeR18vHcI130_assertion description "[It is highly probable that mutations of connexin genes that result in human nonsyndromic deafness cause dysfunction of cochlear gap junctions and thereby interrupt K+ ion recirculation pathways.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP343268.RATMXBHPLzcI5abrNsV207xFBC0DIu2N-n0xUeR18vHcI130_provenance.
- NP1012305.RANz2BDrlkCw-J-S8O8WuAqJYgFCRCTBYEpvk9uiSIjm0130_assertion description "[It is highly probable that mutations of connexin genes that result in human nonsyndromic deafness cause dysfunction of cochlear gap junctions and thereby interrupt K+ ion recirculation pathways.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1012305.RANz2BDrlkCw-J-S8O8WuAqJYgFCRCTBYEpvk9uiSIjm0130_provenance.