Matches in Nanopublications for { ?s ?p "[New mutations in acetylcholine receptor subunit genes reveal heterogeneity in the slow-channel congenital myasthenic syndrome.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine."@en ?g. }
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- NP1136.RAqqW3vjMFtgcw-C5ffQCrDrm1s1psuYJi6qDQT8YXEr4130_assertion description "[New mutations in acetylcholine receptor subunit genes reveal heterogeneity in the slow-channel congenital myasthenic syndrome.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1136.RAqqW3vjMFtgcw-C5ffQCrDrm1s1psuYJi6qDQT8YXEr4130_provenance.
- NP1132.RAedXbbeyvriVl5Uw3Fa6LVesrGjnL84sjU1hKHjrR10E130_assertion description "[New mutations in acetylcholine receptor subunit genes reveal heterogeneity in the slow-channel congenital myasthenic syndrome.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1132.RAedXbbeyvriVl5Uw3Fa6LVesrGjnL84sjU1hKHjrR10E130_provenance.
- NP1144.RAdP8zhUFcBx6TfzP_SBjhdDU7iH9unuTGahsR6JMo8nY130_assertion description "[New mutations in acetylcholine receptor subunit genes reveal heterogeneity in the slow-channel congenital myasthenic syndrome.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1144.RAdP8zhUFcBx6TfzP_SBjhdDU7iH9unuTGahsR6JMo8nY130_provenance.
- NP1121.RA7rWVlj12f4NJ4Ewq6JAgUmSP_WkvEzoCxEPhrtqC4eg130_assertion description "[New mutations in acetylcholine receptor subunit genes reveal heterogeneity in the slow-channel congenital myasthenic syndrome.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1121.RA7rWVlj12f4NJ4Ewq6JAgUmSP_WkvEzoCxEPhrtqC4eg130_provenance.
- assertion description "[New mutations in acetylcholine receptor subunit genes reveal heterogeneity in the slow-channel congenital myasthenic syndrome.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." provenance.
- assertion description "[New mutations in acetylcholine receptor subunit genes reveal heterogeneity in the slow-channel congenital myasthenic syndrome.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." provenance.
- assertion description "[New mutations in acetylcholine receptor subunit genes reveal heterogeneity in the slow-channel congenital myasthenic syndrome.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." provenance.
- assertion description "[New mutations in acetylcholine receptor subunit genes reveal heterogeneity in the slow-channel congenital myasthenic syndrome.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." provenance.
- NP1491.RAD0NE955Zsai5XeYzyWUseHsylSgtaa4W0I2NdOhrNN4130_assertion description "[New mutations in acetylcholine receptor subunit genes reveal heterogeneity in the slow-channel congenital myasthenic syndrome.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1491.RAD0NE955Zsai5XeYzyWUseHsylSgtaa4W0I2NdOhrNN4130_provenance.
- NP9186.RA6bfzkgQ2GmXaXvNLNbK-I-CrMe1ywLXaKVhdq2NsoHM130_assertion description "[New mutations in acetylcholine receptor subunit genes reveal heterogeneity in the slow-channel congenital myasthenic syndrome.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP9186.RA6bfzkgQ2GmXaXvNLNbK-I-CrMe1ywLXaKVhdq2NsoHM130_provenance.