Two novel mutations in the CLCNKB...

BMJ Case Reports 2020 / 07 Vol. 13; Iss. 7

Two novel mutations in the CLCNKB gene leading to classic Bartter syndrome presenting as syncope and hypertension in a 13-year-old boy

Le, Binh T, Duong, Cuong M, Nguyen, Tien Q, Bui, Chi-Bao
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Volume:
13
Journal:
BMJ Case Reports
DOI:
10.1136/bcr-2019-233872
Date:
July, 2020
File:
PDF, 638 KB
2020
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