Matches in Nanopublications for { ?s ?p "[Loss-of-function mutations in TRPM6 are a molecular cause of hypomagnesemia with secondary hypocalcemia, suggesting that TRPM6 is critically involved in transcellular Mg2+ transport in the kidney.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine."@en ?g. }
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- NP828454.RAeeS2DrsrV-Q5ul15w9HH8h5tEhf9nGNszdymreHqEcA130_assertion description "[Loss-of-function mutations in TRPM6 are a molecular cause of hypomagnesemia with secondary hypocalcemia, suggesting that TRPM6 is critically involved in transcellular Mg2+ transport in the kidney.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP828454.RAeeS2DrsrV-Q5ul15w9HH8h5tEhf9nGNszdymreHqEcA130_provenance.
- NP973326.RAQwICofZrb0XuZrZ5oZ2DclWNM5n8s9njfVAcX74lBZs130_assertion description "[Loss-of-function mutations in TRPM6 are a molecular cause of hypomagnesemia with secondary hypocalcemia, suggesting that TRPM6 is critically involved in transcellular Mg2+ transport in the kidney.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP973326.RAQwICofZrb0XuZrZ5oZ2DclWNM5n8s9njfVAcX74lBZs130_provenance.
- assertion description "[Loss-of-function mutations in TRPM6 are a molecular cause of hypomagnesemia with secondary hypocalcemia, suggesting that TRPM6 is critically involved in transcellular Mg2+ transport in the kidney.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." provenance.
- NP806363.RA2st4QIKmS80awxoLcnQIuR0Wn_jE-9ivge-_GiyqpT4130_assertion description "[Loss-of-function mutations in TRPM6 are a molecular cause of hypomagnesemia with secondary hypocalcemia, suggesting that TRPM6 is critically involved in transcellular Mg2+ transport in the kidney.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP806363.RA2st4QIKmS80awxoLcnQIuR0Wn_jE-9ivge-_GiyqpT4130_provenance.