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Short Report
A homozygous founder mutation in TRAPPC6B associates with a neurodevelopmental disorder characterised by microcephaly, epilepsy and autistic features

 

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Jun 201745812246
Jul 20174345328
Aug 20172474526
Sep 20171642517
Oct 2017148299
Nov 2017119185
Dec 20173553620
Jan 20184404423
Feb 20181712917
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Sep 2018125179
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Mar 20198153
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Jan 202078113
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Apr 20203310
May 20205333
Jun 20206444
Jul 20209874
Aug 20204511
Total5220709369