Article révisé par les pairs
Titre:
  • Hyperekplexia in Kurdish families: a possible GLRA1 founder mutation.
Auteur:Sirén, A; Legros, Benjamin; Chahine, Lyne; Misson, J-P; Pandolfo, Massimo
Informations sur la publication:Neurology, 67, 1, page (137-139)
Statut de publication:Publié, 2006-07
Sujet CREF:Sciences bio-médicales et agricoles
MeSH keywords:Adolescent
Adult
Child, Preschool
DNA Mutational Analysis -- methods
Exons
Family Health
Female
Genetic Predisposition to Disease
Humans
Male
Mutation
Pedigree
Receptors, Glycine -- genetics
Stiff-Person Syndrome -- genetics
Turkey
Note générale:Comparative Study
Journal Article
Research Support, Non-U.S. Gov't
Langue:Anglais
Identificateurs:urn:issn:0028-3878
info:doi/10.1212/01.wnl.0000223347.73493.af
info:pii/67/1/137
info:scp/33746811061
info:pmid/16832093