Burden of de novo mutations and inherited rare single nucleotide variants in children with sensory processing dysfunction
Pre-publication versions of this article are available by contacting firstname.lastname@example.org.
|19 Jan 2018||Submitted||Original manuscript|
|19 Feb 2018||Reviewed||Reviewer Report - Carl Ernst|
|27 Feb 2018||Reviewed||Reviewer Report - Yin Yao|
|30 Mar 2018||Author responded||Author comments - Elysa Marco|
|Resubmission - Version 2|
|30 Mar 2018||Submitted||Manuscript version 2|
|20 Apr 2018||Author responded||Author comments - Elysa Marco|
|Resubmission - Version 3|
|20 Apr 2018||Submitted||Manuscript version 3|
|26 Apr 2018||Editorially accepted|
|25 May 2018||Article published||10.1186/s12920-018-0362-x|
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