Mimicry and well known genetic friends: molecular diagnosis in an Iranian cohort of suspected Bartter syndrome and proposition of an algorithm for clinical differential diagnosis

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Authors: Maryam Najafi, Dor Mohammad Kordi-Tamandani, Farkhondeh Behjati, Simin Sadeghi-Bojd, Zeineb Bakey, Ehsan Ghayoor Karimiani, Isabel Schüle, Anoush Azarfar, Miriam Schmidts

Journal title: Orphanet Journal of Rare Diseases

Journal number: 14/1

Journal publisher: BioMed Central

Published year: 2019

DOI identifier: 10.1186/s13023-018-0981-5

ISSN: 1750-1172