Matches in Nanopublications for { ?s ?p "[Constitutively activating thyrotropin receptor (TSHR) germline mutations have been identified as a molecular cause of congenital hyperthyroidism.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine."@en ?g. }
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- NP830176.RAp05eWsLYs4WIvIY-R73tYZlWUdIFpT4uNJnojje8b6M130_assertion description "[Constitutively activating thyrotropin receptor (TSHR) germline mutations have been identified as a molecular cause of congenital hyperthyroidism.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP830176.RAp05eWsLYs4WIvIY-R73tYZlWUdIFpT4uNJnojje8b6M130_provenance.
- NP609469.RAzP2N5Bbi9Y-tTikmfsXalV8FnO5Qelwuix3uflxHErA130_assertion description "[Constitutively activating thyrotropin receptor (TSHR) germline mutations have been identified as a molecular cause of congenital hyperthyroidism.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP609469.RAzP2N5Bbi9Y-tTikmfsXalV8FnO5Qelwuix3uflxHErA130_provenance.
- NP760782.RAqATaD47uPVcyB7SYfKw4f3M3peSCypeOyDs-Y7nhRuQ130_assertion description "[Constitutively activating thyrotropin receptor (TSHR) germline mutations have been identified as a molecular cause of congenital hyperthyroidism.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP760782.RAqATaD47uPVcyB7SYfKw4f3M3peSCypeOyDs-Y7nhRuQ130_provenance.
- NP675101.RAurCdt5vTWK0yIMtAPe_ZEkcKgHAHnNbf4zxOlnqn_6w130_assertion description "[Constitutively activating thyrotropin receptor (TSHR) germline mutations have been identified as a molecular cause of congenital hyperthyroidism.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP675101.RAurCdt5vTWK0yIMtAPe_ZEkcKgHAHnNbf4zxOlnqn_6w130_provenance.