Matches in Nanopublications for { ?s ?p "[Heterozygous inactivating mutations of the calcium-sensing receptor (CaR) gene cause familial hypocalciuric hypercalcaemia (FHH), a generally benign disorder characterized by mild to moderate PTH-dependent hypercalcaemia.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine."@en ?g. }
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- NP323738.RAZWkFk5LbKROE3lUa4tVa-py4yo0Ocn8p1xrQZetRykE130_assertion description "[Heterozygous inactivating mutations of the calcium-sensing receptor (CaR) gene cause familial hypocalciuric hypercalcaemia (FHH), a generally benign disorder characterized by mild to moderate PTH-dependent hypercalcaemia.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP323738.RAZWkFk5LbKROE3lUa4tVa-py4yo0Ocn8p1xrQZetRykE130_provenance.
- NP264270.RAESU1ZtFQGDBhd11GK7vsViwtCr5FQUn82RUvbaEL6sk130_assertion description "[Heterozygous inactivating mutations of the calcium-sensing receptor (CaR) gene cause familial hypocalciuric hypercalcaemia (FHH), a generally benign disorder characterized by mild to moderate PTH-dependent hypercalcaemia.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP264270.RAESU1ZtFQGDBhd11GK7vsViwtCr5FQUn82RUvbaEL6sk130_provenance.
- NP547611.RAbCC6CtdSv8chtHRXxWkKD0EJli9N-ZEZQZw5x1OGSGs130_assertion description "[Heterozygous inactivating mutations of the calcium-sensing receptor (CaR) gene cause familial hypocalciuric hypercalcaemia (FHH), a generally benign disorder characterized by mild to moderate PTH-dependent hypercalcaemia.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP547611.RAbCC6CtdSv8chtHRXxWkKD0EJli9N-ZEZQZw5x1OGSGs130_provenance.
- NP547609.RAKstMnAtpcdL2GK9T9ACm-SgrFe4i__tbkddhstSJby0130_assertion description "[Heterozygous inactivating mutations of the calcium-sensing receptor (CaR) gene cause familial hypocalciuric hypercalcaemia (FHH), a generally benign disorder characterized by mild to moderate PTH-dependent hypercalcaemia.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP547609.RAKstMnAtpcdL2GK9T9ACm-SgrFe4i__tbkddhstSJby0130_provenance.
- NP972559.RA51dJIAYo0o1LSDpbYWWSAgBjTa92ddkbpE9t-MhX39U130_assertion description "[Heterozygous inactivating mutations of the calcium-sensing receptor (CaR) gene cause familial hypocalciuric hypercalcaemia (FHH), a generally benign disorder characterized by mild to moderate PTH-dependent hypercalcaemia.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP972559.RA51dJIAYo0o1LSDpbYWWSAgBjTa92ddkbpE9t-MhX39U130_provenance.