Detection of a Novel Mutation in the GAA Gene in an Iranian Child with Glycogen Storage Disease Type II Article

Galehdari, Hamid, Emami, Mozhgan, Mohammadian, Gholamreza et al. (2013). Detection of a Novel Mutation in the GAA Gene in an Iranian Child with Glycogen Storage Disease Type II . 16(2), 126-128.

cited authors

  • Galehdari, Hamid; Emami, Mozhgan; Mohammadian, Gholamreza; Khodadadi, Ali; Azmoon, Somayeh; Baradaran, Masumeh

authors

publication date

  • February 1, 2013

keywords

  • Acid alpha-glucosidase
  • General & Internal Medicine
  • Iranian
  • Life Sciences & Biomedicine
  • Medicine, General & Internal
  • Pompe disease
  • Science & Technology
  • glycogen storage disorder type II
  • novel mutation

publisher

  • ACAD MEDICAL SCIENCES I R IRAN

start page

  • 126

end page

  • 128

volume

  • 16

issue

  • 2