Matches in Nanopublications for { ?s ?p "[Loss-of-function mutations in the KCNJ2 cause approximately 50% of Andersen-Tawil Syndrome (ATS) characterized by a classic triad of periodic paralysis, ventricular arrhythmia, and dysmorphic features.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine."@en ?g. }
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- NP862127.RAaXGOnEXpuMnOqQMzDpWGh2J2tEZ9A_ijJERXXKZqRhs130_assertion description "[Loss-of-function mutations in the KCNJ2 cause approximately 50% of Andersen-Tawil Syndrome (ATS) characterized by a classic triad of periodic paralysis, ventricular arrhythmia, and dysmorphic features.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP862127.RAaXGOnEXpuMnOqQMzDpWGh2J2tEZ9A_ijJERXXKZqRhs130_provenance.
- NP621001.RABix00dGKDEfvGx6ouFOgh2MBU-azZqiFjKg93ibgZ0U130_assertion description "[Loss-of-function mutations in the KCNJ2 cause approximately 50% of Andersen-Tawil Syndrome (ATS) characterized by a classic triad of periodic paralysis, ventricular arrhythmia, and dysmorphic features.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP621001.RABix00dGKDEfvGx6ouFOgh2MBU-azZqiFjKg93ibgZ0U130_provenance.
- NP763650.RA8hVMMryONuxJEabTE7OyQXlleCXJYJkvR04Ae8IJdic130_assertion description "[Loss-of-function mutations in the KCNJ2 cause approximately 50% of Andersen-Tawil Syndrome (ATS) characterized by a classic triad of periodic paralysis, ventricular arrhythmia, and dysmorphic features.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP763650.RA8hVMMryONuxJEabTE7OyQXlleCXJYJkvR04Ae8IJdic130_provenance.
- NP597424.RAAPlskruePi9Al5y4ocX980KBaT7CsnapEgDo045sObE130_assertion description "[Loss-of-function mutations in the KCNJ2 cause approximately 50% of Andersen-Tawil Syndrome (ATS) characterized by a classic triad of periodic paralysis, ventricular arrhythmia, and dysmorphic features.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP597424.RAAPlskruePi9Al5y4ocX980KBaT7CsnapEgDo045sObE130_provenance.
- NP522319.RAVCnYgbyM5L2CxfyhWGnqaGLxFg9YDFNVAgx5l2sdkBI130_assertion description "[Loss-of-function mutations in the KCNJ2 cause approximately 50% of Andersen-Tawil Syndrome (ATS) characterized by a classic triad of periodic paralysis, ventricular arrhythmia, and dysmorphic features.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP522319.RAVCnYgbyM5L2CxfyhWGnqaGLxFg9YDFNVAgx5l2sdkBI130_provenance.
- NP522360.RAdCTDBrHk1RRyiY9KzVc1TnI7tx23M6ssnSVve5rhqSw130_assertion description "[Loss-of-function mutations in the KCNJ2 cause approximately 50% of Andersen-Tawil Syndrome (ATS) characterized by a classic triad of periodic paralysis, ventricular arrhythmia, and dysmorphic features.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP522360.RAdCTDBrHk1RRyiY9KzVc1TnI7tx23M6ssnSVve5rhqSw130_provenance.
- NP597425.RA2SYHVm4rlRrfW7UBEsi_IuR7cXBonDwYWGAkqTPChm8130_assertion description "[Loss-of-function mutations in the KCNJ2 cause approximately 50% of Andersen-Tawil Syndrome (ATS) characterized by a classic triad of periodic paralysis, ventricular arrhythmia, and dysmorphic features.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP597425.RA2SYHVm4rlRrfW7UBEsi_IuR7cXBonDwYWGAkqTPChm8130_provenance.
- NP597426.RA9KX-zTlWAHoFXUR2i0qXoZFa4ofANeMP9QsMoFrWySw130_assertion description "[Loss-of-function mutations in the KCNJ2 cause approximately 50% of Andersen-Tawil Syndrome (ATS) characterized by a classic triad of periodic paralysis, ventricular arrhythmia, and dysmorphic features.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP597426.RA9KX-zTlWAHoFXUR2i0qXoZFa4ofANeMP9QsMoFrWySw130_provenance.
- assertion description "[Loss-of-function mutations in the KCNJ2 cause approximately 50% of Andersen-Tawil Syndrome (ATS) characterized by a classic triad of periodic paralysis, ventricular arrhythmia, and dysmorphic features.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." provenance.
- assertion description "[Loss-of-function mutations in the KCNJ2 cause approximately 50% of Andersen-Tawil Syndrome (ATS) characterized by a classic triad of periodic paralysis, ventricular arrhythmia, and dysmorphic features.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." provenance.
- assertion description "[Loss-of-function mutations in the KCNJ2 cause approximately 50% of Andersen-Tawil Syndrome (ATS) characterized by a classic triad of periodic paralysis, ventricular arrhythmia, and dysmorphic features.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." provenance.
- NP522348.RAtKxJOPjxbv8S6euaxvsKko_6jrCa8jMrIznOhXk0fkc130_assertion description "[Loss-of-function mutations in the KCNJ2 cause approximately 50% of Andersen-Tawil Syndrome (ATS) characterized by a classic triad of periodic paralysis, ventricular arrhythmia, and dysmorphic features.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP522348.RAtKxJOPjxbv8S6euaxvsKko_6jrCa8jMrIznOhXk0fkc130_provenance.