Article info

PDF
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
  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

Publication history

  • Received 1 May 2007
  • Revised 26 June 2007
  • Accepted 26 June 2007
  • Published in print 1 November 2007.
  • Published first 6 July 2007.

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.