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PubMed (cited) for id: 601814

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Recurrent FXYD2 p.Gly41Arg mutation in patients with isolated dominant hypomagnesaemia.
de Baaij JH, Dorresteijn EM, Hennekam EA, Kamsteeg EJ, Meijer R, Dahan K, Muller M, van den Dorpel MA, Bindels RJ, Hoenderop JG, Devuyst O, Knoers NV. de Baaij JH, et al. Nephrol Dial Transplant. 2015 Jun;30(6):952-7. doi: 10.1093/ndt/gfv014. Epub 2015 Mar 11. Nephrol Dial Transplant. 2015. PMID: 25765846 Free article.
Crystal structure of the sodium-potassium pump.
Morth JP, Pedersen BP, Toustrup-Jensen MS, Sørensen TL, Petersen J, Andersen JP, Vilsen B, Nissen P. Morth JP, et al. Nature. 2007 Dec 13;450(7172):1043-9. doi: 10.1038/nature06419. Nature. 2007. PMID: 18075585
The gene for glycogen-storage disease type 1b maps to chromosome 11q23.
Annabi B, Hiraiwa H, Mansfield BC, Lei KJ, Ubagai T, Polymeropoulos MH, Moses SW, Parvari R, Hershkovitz E, Mandel H, Fryman M, Chou JY. Annabi B, et al. Am J Hum Genet. 1998 Feb;62(2):400-5. doi: 10.1086/301727. Am J Hum Genet. 1998. PMID: 9463334 Free PMC article.