Open AccessDifferential diagnosis of classical Bartter syndrome and Gitelman syndrome: Do we need genetic analysis?
Author(s) -
Serçin Güven,
İbrahim Gökçe,
Ceren Alavanda,
Neslihan Çiçek,
Ece Bodur Demirci,
Mehtap Sak,
Serim Pul,
Özde Nisa Türkkan,
Nurdan Yıldız,
Pınar Ata,
Harika Alpay
Publication year - 2021
Publication title -
marmara medical journal
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.112
H-Index - 11
ISSN - 1019-1941
DOI - 10.5472/marumj.1012351
Subject(s) - medicine , bartter syndrome , gitelman syndrome , missense mutation , compound heterozygosity , gastroenterology , creatinine , hypokalemia , bartter's syndrome , nonsense mutation , hypocalciuria , renal function , endocrinology , hypomagnesemia , pediatrics , mutation , genetics , gene , biology , magnesium , materials science , metallurgy
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