Article info

Download PDFPDF
Original article
Homozygous missense mutation in MED25 segregates with syndromic intellectual disability in a large consanguineous family

Authors

  1. 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
View Full Text

Citation

Figueiredo T, Melo US, Pessoa ALS, et al
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 
January 19, 2015

Article Versions

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.