Matches in Nanopublications for { ?s ?p "[The hypocalciuric, hypomagnesemic variant of Bartter syndrome (Gitelman syndrome), presents in early adulthood with predominantly musculoskeletal symptoms and is due to mutations in the gene encoding the Na-Cl cotransporter (NCCT).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine."@en ?g. }
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- NP609275.RA3VW3rlhcxyyJLjAg7d7bna0px-u9KoL9rrq3vTYNwNM130_assertion description "[The hypocalciuric, hypomagnesemic variant of Bartter syndrome (Gitelman syndrome), presents in early adulthood with predominantly musculoskeletal symptoms and is due to mutations in the gene encoding the Na-Cl cotransporter (NCCT).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP609275.RA3VW3rlhcxyyJLjAg7d7bna0px-u9KoL9rrq3vTYNwNM130_provenance.
- NP700427.RAVL-Jha28uCmtyhFdtK5ZSm3oEoo-S_c5nrsJa2GKaUs130_assertion description "[The hypocalciuric, hypomagnesemic variant of Bartter syndrome (Gitelman syndrome), presents in early adulthood with predominantly musculoskeletal symptoms and is due to mutations in the gene encoding the Na-Cl cotransporter (NCCT).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP700427.RAVL-Jha28uCmtyhFdtK5ZSm3oEoo-S_c5nrsJa2GKaUs130_provenance.
- assertion description "[The hypocalciuric, hypomagnesemic variant of Bartter syndrome (Gitelman syndrome), presents in early adulthood with predominantly musculoskeletal symptoms and is due to mutations in the gene encoding the Na-Cl cotransporter (NCCT).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." provenance.
- NP341298.RAutin-6tUWN4c7dbwmtHGVw2JvYkJlVA4IQ770lHPLRk130_assertion description "[The hypocalciuric, hypomagnesemic variant of Bartter syndrome (Gitelman syndrome), presents in early adulthood with predominantly musculoskeletal symptoms and is due to mutations in the gene encoding the Na-Cl cotransporter (NCCT).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP341298.RAutin-6tUWN4c7dbwmtHGVw2JvYkJlVA4IQ770lHPLRk130_provenance.
- NP341299.RA4grIW2Yhcu_BsSXFqdANa_pRF4F5ZcfF1RdetJSVmho130_assertion description "[The hypocalciuric, hypomagnesemic variant of Bartter syndrome (Gitelman syndrome), presents in early adulthood with predominantly musculoskeletal symptoms and is due to mutations in the gene encoding the Na-Cl cotransporter (NCCT).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP341299.RA4grIW2Yhcu_BsSXFqdANa_pRF4F5ZcfF1RdetJSVmho130_provenance.