Article info
New loci
Original article
Homozygous missense mutation in MED25 segregates with syndromic intellectual disability in a large consanguineous family
- Correspondence to Professor Silvana Santos, Department of Biology, Paraíba State University, Rua das Baraúnas, 351, Bodocongó, Campina Grande, Paraiba 58.410-367, Brazil; silvanasantos{at}ccbs.uepb.edu.br
Citation
Homozygous missense mutation in MED25 segregates with syndromic intellectual disability in a large consanguineous family
Publication history
- Received September 24, 2014
- Revised November 25, 2014
- Accepted November 26, 2014
- First published December 19, 2014.
Online issue publication
April 27, 2016
Article Versions
- Previous version (27 April 2016).
- You are viewing the most recent version of this article.
Request permissions
If you wish to reuse any or all of this article please use the link below which will take you to the Copyright Clearance Center’s RightsLink service. You will be able to get a quick price and instant permission to reuse the content in many different ways.
Copyright information
Published by the BMJ Publishing Group Limited. For permission to use (where not already granted under a licence) please go to http://group.bmj.com/group/rights-licensing/permissions