You are here

  • Home
  • Archive
  • Volume 44, Issue 11
  • Mutations in the AP1S2 gene encoding the sigma 2 subunit of the adaptor protein 1 complex are associated with syndromic X-linked mental retardation with hydrocephalus and calcifications in basal ganglia

Article info

Article menu
Download PDFPDF
Letters to JMG
Mutations in the AP1S2 gene encoding the sigma 2 subunit of the adaptor protein 1 complex are associated with syndromic X-linked mental retardation with hydrocephalus and calcifications in basal ganglia

Authors

  1. Dr Thierry Bienvenu, Institut Cochin, Université Paris Descartes, CNRS (UMR 8104), Paris, France; bienvenu{at}cochin.inserm.fr
View Full Text

Citation

Saillour Y, Zanni G, Des Portes V, et al
Mutations in the AP1S2 gene encoding the sigma 2 subunit of the adaptor protein 1 complex are associated with syndromic X-linked mental retardation with hydrocephalus and calcifications in basal ganglia
Journal of Medical Genetics 2007;44:739-744.

Publication history

  • Received May 1, 2007
  • Revised June 26, 2007
  • Accepted June 26, 2007
  • First published July 6, 2007.
Online issue publication 
April 27, 2016

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.

Copyright information

2007 BMJ Publishing Group Ltd