You are here

Article info

Article menu

Download PDFPDF

Original article
SPRED1 germline mutations caused a neurofibromatosis type 1 overlapping phenotype
Free

Authors

  1. Dr E Pasmant, UMR745 INSERM, Université Paris Descartes, Faculté des Sciences Pharmaceutiques et Biologiques, 4 avenue de l’Observatoire, 75006, Paris, France; eric.pasmant{at}etu.univ-paris5.fr
View Full Text

Citation

Pasmant E, Sabbagh A, Hanna N, et al
SPRED1 germline mutations caused a neurofibromatosis type 1 overlapping phenotype
Journal of Medical Genetics 2009;46:425-430.

Publication history

  • Received December 11, 2008
  • Revised February 6, 2009
  • Accepted February 11, 2009
  • First published April 14, 2009.
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

2009 BMJ Publishing Group Ltd