Spin label study of erythrocyte membrane fluidity in myotonic and Duchenne muscular dystrophy and congenital myotonia Academic Article Article uri icon

Overview

MeSH Major

  • Amyotrophic Lateral Sclerosis
  • Immunotherapy
  • Neuroimmunomodulation
  • Parkinson Disease
  • T-Lymphocytes, Regulatory

abstract

  • INTACT erythrocyte membranes from patients with myotonic muscular dystrophy (MMD) have been shown by spin labelling (review of method in ref. 1) to have greater membrane surface fluidity than normal2,3. We have now evaluated the specificity of this phenomenon. We used erythrocytes from patients with MMD, and also from patients with Duchenne muscular dystrophy (DMD), as a model of dystrophy with no myotonia, and from patients with congenital myotonia (CM) as a model of myotonia without dystrophy. © 1976 Nature Publishing Group.

publication date

  • December 1976

Research

keywords

  • Academic Article

Identity

Digital Object Identifier (DOI)

  • 10.1038/263159a0

PubMed ID

  • 184394

Additional Document Info

start page

  • 159

end page

  • 61

volume

  • 263

number

  • 5573