Article révisé par les pairs
Titre:
  • Mutation of a potassium channel-related gene in progressive myoclonic epilepsy.
Auteur:Van Bogaert, Patrick; Azizieh, Naïm-Régis; Désir, Julie; Aeby, Alec; De Meirleir, Linda; Laes, Jean-François; Christiaens, Florence; Abramowicz, Marc
Informations sur la publication:Annals of neurology, 61, 6, page (579-586)
Statut de publication:Publié, 2007-06
Sujet CREF:Sciences bio-médicales et agricoles
MeSH keywords:Adolescent
Amino Acid Sequence
Child
Child, Preschool
Consanguinity
DNA Mutational Analysis
Disease Progression
Epilepsies, Myoclonic -- diagnosis
Epilepsies, Myoclonic -- genetics
Female
Homozygote
Humans
Male
Molecular Sequence Data
Morocco
Mutation -- genetics
Pedigree
Potassium Channels -- genetics
Sequence Homology, Amino Acid
Note générale:Journal Article
Research Support, Non-U.S. Gov't
FLWIN
Langue:Anglais
Identificateurs:urn:issn:0364-5134
info:doi/10.1002/ana.21121
info:scp/34447522241
info:pmid/17455289

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