Analysis of mutations of two Gitelman syndrome family SLC12A3 genes and proposed treatments using Chinese medicine

Analysis of mutations of two Gitelman syndrome family SLC12A3 genes and proposed treatments using... Chin J Integr Med 2017 Jun;23(6):461-468 • • Available online at link.springer.com/journal/11655 hinese Journal of Integrative Medicine Journal homepage: www.cjim.cn/zxyjhen/zxyjhen/ch/index.aspx E-mail: cjim_en@cjim.cn Original Article Analysis of Mutations of Two Gitelman Syndrome Family SLC12A3 Genes and Proposed Treatments Using Chinese Medicine 1 1 3 2 LUO Jie-wei , MENG Xiao-rong , YANG Xiao , LIANG Ji-xing , 2 1 4 HONG Fu-yuan , ZHENG Xing-yu , and LI Wei-hua O Objective bjective A ABSTRACT BSTRACT : : To determine the gene location of two Gitelman syndrome (GS) family SLC12A3 genes and To determine the gene location of two Gitelman syndrome (GS) family SLC12A3 genes and e explore treatments using Chinese medicine (CM) prescriptions. xplore treatments using Chinese medicine (CM) prescriptions. M Methods ethods:: In order to locate the two GS mutations, In order to locate the two GS mutations, s samples were collected from 11 people from two different pedigrees for direct genetic sequencing and comparison amples were collected from 11 people from two different pedigrees for direct genetic sequencing and comparison o of the 26 exons of SLC12A3. Furthermore, the change of serum potassium was monitored throughout the therapy f the 26 exons of SLC12A3. Furthermore, the change of http://www.deepdyve.com/assets/images/DeepDyve-Logo-lg.png Chinese Journal of Integrative Medicine Springer Journals

Analysis of mutations of two Gitelman syndrome family SLC12A3 genes and proposed treatments using Chinese medicine

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Publisher
Springer Berlin Heidelberg
Copyright
Copyright © 2016 by Chinese Association of the Integration of Traditional and Western Medicine and Springer-Verlag Berlin Heidelberg
Subject
Medicine & Public Health; Medicine/Public Health, general
ISSN
1672-0415
eISSN
1993-0402
D.O.I.
10.1007/s11655-016-2461-x
Publisher site
See Article on Publisher Site

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