Exonic CLDN16 mutations associated with familial hypomagnesemia with hypercalciuria and nephrocalcinosis can induce deleterious mRNA alterations
Pre-publication versions of this article are available by contacting email@example.com.
|26 Jul 2018||Submitted||Original manuscript|
|28 Aug 2018||Reviewed||Reviewer Report - D. Iancu|
|26 Sep 2018||Reviewed||Reviewer Report - Shaogen Wu|
|8 Oct 2018||Author responded||Author comments - Ana Perdomo-Ramirez|
|Resubmission - Version 2|
|8 Oct 2018||Submitted||Manuscript version 2|
|9 Oct 2018||Reviewed||Reviewer Report - Shaogen Wu|
|21 Oct 2018||Reviewed||Reviewer Report - D. Iancu|
|Resubmission - Version 3|
|Submitted||Manuscript version 3|
|30 Oct 2018||Editorially accepted|
|8 Jan 2019||Article published||10.1186/s12881-018-0713-7|
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