Matches in Nanopublications for { ?s ?p "[We describe an inherited, autosomal-dominant form of sinus node dysfunction caused by a missense mutation in the HCN4 ion channel pore.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine."@en ?g. }
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- NP805580.RAQ9Muq4yU434JttNGsKUpZy2CX8v4ns9cMW6NOE3rqmQ130_assertion description "[We describe an inherited, autosomal-dominant form of sinus node dysfunction caused by a missense mutation in the HCN4 ion channel pore.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP805580.RAQ9Muq4yU434JttNGsKUpZy2CX8v4ns9cMW6NOE3rqmQ130_provenance.
- NP621329.RA6hFjmKJ-KkB-gQhkZTdQXIO4CqeqjP84SaMg8nxcuLA130_assertion description "[We describe an inherited, autosomal-dominant form of sinus node dysfunction caused by a missense mutation in the HCN4 ion channel pore.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP621329.RA6hFjmKJ-KkB-gQhkZTdQXIO4CqeqjP84SaMg8nxcuLA130_provenance.
- NP835205.RAmqfJWE6E09l0IMjprmX7ZjQRj2_ZBcBjEjy5gsCMGMQ130_assertion description "[We describe an inherited, autosomal-dominant form of sinus node dysfunction caused by a missense mutation in the HCN4 ion channel pore.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP835205.RAmqfJWE6E09l0IMjprmX7ZjQRj2_ZBcBjEjy5gsCMGMQ130_provenance.