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- ng0196-24 accessdate "2014-11-08".
- ng0196-24 author "Simon DB, Nelson-Williams C, Bia MJ, Ellison D, Karet FE, Molina AM, Vaara I, Iwata F, Cushner HM, Koolen M, Gainza FJ, Gitleman HJ, Lifton RP".
- ng0196-24 date "Jan 1996".
- ng0196-24 date "January 1996".
- ng0196-24 displayAuthors "etal".
- ng0196-24 doi "10.1038/ng0196-24".
- ng0196-24 first1 "DB".
- ng0196-24 first2 "C".
- ng0196-24 isCitedBy Gitelman_syndrome.
- ng0196-24 isCitedBy Magnesium_deficiency_(medicine).
- ng0196-24 issue "1".
- ng0196-24 journal "Nat Genet".
- ng0196-24 journal "Nat. Genet.".
- ng0196-24 last1 "Simon".
- ng0196-24 last2 "Nelson-Williams".
- ng0196-24 pages "24–30".
- ng0196-24 pmid "8528245".
- ng0196-24 title "Gitelman's variant of Bartter's syndrome, inherited hypokalaemic alkalosis, is caused by mutations in the thiazide-sensitive Na-Cl cotransporter".
- ng0196-24 title "Gitelman's variant of Bartter's syndrome, inherited hypokalaemic alkalosis, is caused by mutations in the thiazide-sensitive Na-Cl cotransporter.".
- ng0196-24 url "http://www.ncbi.nlm.nih.gov/pubmed?term=david%20b%20simon%20gitelman%27s%20variant".
- ng0196-24 url pubmed?term=david%20b%20simon%20gitelmans%20variant.
- ng0196-24 volume "12".