%0 Journal Article
%T 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
%A Anoush Azarfar
%A Dor Mohammad Kordi-Tamandani
%A Ehsan Ghayoor Karimiani
%A Farkhondeh Behjati
%A Isabel Sch¨šle
%A Maryam Najafi
%A Miriam Schmidts
%A Simin Sadeghi-Bojd
%A Zeineb Bakey
%J Archive of "Orphanet Journal of Rare Diseases".
%D 2019
%R 10.1186/s13023-018-0981-5
%X The online version of this article (10.1186/s13023-018-0981-5) contains supplementary material, which is available to authorized users
%K Bartter syndrome
%K Whole exome sequencing
%K Pseudo-Bartter-syndrome
%U https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6375149/