A comparison of central nervous system involvement in patients with classical Fabry disease or the later-onset subtype with the IVS4+919G>A mutation
Pre-publication versions of this article are available by contacting email@example.com.
|22 Apr 2016||Submitted||Original manuscript|
|14 Jun 2016||Reviewed||Reviewer Report - Dawn A Laney|
|26 Jun 2016||Reviewed||Reviewer Report - Hiroaki Adachi|
|2 Sep 2016||Author responded||Author comments - Han-Jui Lee|
|Resubmission - Version 2|
|2 Sep 2016||Submitted||Manuscript version 2|
|2 Oct 2016||Reviewed||Reviewer Report - Hiroaki Adachi|
|23 Jan 2017||Author responded||Author comments - Han-Jui Lee|
|Resubmission - Version 3|
|23 Jan 2017||Submitted||Manuscript version 3|
|26 Jan 2017||Editorially accepted|
|6 Feb 2017||Article published||10.1186/s12883-017-0810-9|
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