Literature DB >> 17882248

The Gitelman syndrome mutation, IVS9+1G>T, is common across Europe.

S T Bouwer, E Coto, F Santos, D Angelicheva, D Chandler, L Kalaydjieva.   

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Year:  2007        PMID： 17882248     DOI： 10.1038/sj.ki.5002504

Source DB:  PubMed          Journal:  Kidney Int        ISSN： 0085-2538            Impact factor:   10.612


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  4 in total

1.  Clinical utility gene card for: Gitelman syndrome.

Authors:  Nine Vam Knoers; Olivier Devuyst; Erik-Jan Kamsteeg
Journal:  Eur J Hum Genet       Date:  2011-02-23       Impact factor: 4.246

Review 2.  A novel SLC12A3 gene homozygous mutation of Gitelman syndrome in an Asian pedigree and literature review.

Authors:  Q Lü; Y Zhang; C Song; Z An; S Wei; J Huang; L Huang; L Tang; N Tong
Journal:  J Endocrinol Invest       Date:  2015-08-11       Impact factor: 4.256

Review 3.  A novel SLC12A3 homozygous c2039delG mutation in Gitelman syndrome with hypocalcemia.

Authors:  Wenjun Yang; Shaoli Zhao; Yanhong Xie; Zhaohui Mo
Journal:  BMC Nephrol       Date:  2018-12-17       Impact factor: 2.388

4.  Consideration of the diagnosis of hypertension accompanied with hypokalaemia: monism or dualism?

Authors:  Qingguo Lü; Yajie Dong; Heng Wan; Yuwei Zhang; Lizhi Tang; Fang Zhang; Zhe Yan; Nanwei Tong
Journal:  J Int Med Res       Date:  2018-05-29       Impact factor: 1.671
  4 in total

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