A novel splicing mutation in CLCNKB in a Chinese patient with Bartter syndrome type III.
- Author:
Yan DONG
1
;
Gang JI
;
Qi-Wen FENG
;
Xian-Ting ZENG
;
Geng-Ru JIANG
Author Information
1. Department of Endocrinology, Xinhua Hospital, Shanghai Jiao Tong University School of Medicine, Shanghai 200092, China.
- Publication Type:Case Reports
- MeSH:
Asian Continental Ancestry Group;
Bartter Syndrome;
genetics;
Child;
Chloride Channels;
genetics;
Humans;
Male;
Mutation
- From:
Chinese Medical Journal
2010;123(21):3151-3153
- CountryChina
- Language:English
