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

Overview of attention for article published in Orphanet Journal of Rare Diseases, February 2019

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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. https://t.co/cK8dum5bhZ

20 Apr 2019

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20 Apr 2019

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New from #ERC_Research https://t.co/10oRX7UXr9 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

05 Mar 2019

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