You are here

  • Home
  • Online First
  • Autosomal recessive corneal endothelial dystrophy (CHED2) is associated with mutations in SLC4A11

Article Text

Article menu

See original article:

other Versions

Download PDFPDF
Letters to JMG
Autosomal recessive corneal endothelial dystrophy (CHED2) is associated with mutations in SLC4A11

https://doi.org/10.1136/jmg.2006.044644

Statistics from Altmetric.com

    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.

    PDF extract preview

    This is a PDF-only article. The first page of the PDF of this article appears above.

    Linked Articles

    • Miscellaneous
      CORRECTION
      BMJ Publishing Group Ltd
      Journal of Medical Genetics 2007; 44 407-407 Published Online First: 05 Jun 2007. doi: 10.1136/jmg.2007.044644corr1