You are here

  • Home
  • Archive
  • Volume 36, Issue 1
  • Frequency of mutations for glycogen storage disease type II in different populations: the Δ525T and Δexon 18 mutations are not generally “common” in white populations

Article info

Article menu
Letters to the editor
Frequency of mutations for glycogen storage disease type II in different populations: the Δ525T and Δexon 18 mutations are not generally “common” in white populations

Authors

    View Full Text

    Citation

    HIRSCHHORN R, HUIE ML
    Frequency of mutations for glycogen storage disease type II in different populations: the Δ525T and Δexon 18 mutations are not generally “common” in white populations
    Journal of Medical Genetics 1999;36:85-86.

    Publication history

    • First published January 1, 1999.
    Online issue publication 
    April 27, 2016

    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

    Journal of Medical Genetics