A novel splicing mutation in the PKD1 gene causes autosomal dominant polycystic kidney disease in a Chinese family: a case report
Pre-publication versions of this article are available by contacting firstname.lastname@example.org.
|22 Jul 2018||Submitted||Original manuscript|
|27 Aug 2018||Reviewed||Reviewer Report - Éliane Chouery|
|28 Aug 2018||Reviewed||Reviewer Report - Sulman Basit|
|15 Sep 2018||Author responded||Author comments - Peiwen Xu|
|Resubmission - Version 2|
|15 Sep 2018||Submitted||Manuscript version 2|
|3 Oct 2018||Reviewed||Reviewer Report - Éliane Chouery|
|5 Oct 2018||Reviewed||Reviewer Report - Amrik Sahota|
|16 Oct 2018||Author responded||Author comments - Peiwen Xu|
|Resubmission - Version 3|
|16 Oct 2018||Submitted||Manuscript version 3|
|22 Oct 2018||Editorially accepted|
|13 Nov 2018||Article published||10.1186/s12881-018-0706-6|
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