Severe episodic neurological deficits and permanent mental retardation in a child with a novel FHM2ATP1A2mutation-Reference-Cited by-同舟云学术

Severe episodic neurological deficits and permanent mental retardation in a child with a novel FHM2ATP1A2mutation

Published:2006-01-25 Issue:2 Volume:59 Page:310-314
ISSN:0364-5134
Container-title:Annals of Neurology
language:en
Short-container-title:Ann Neurol.

Author:

Vanmolkot K. R. J.¹,Stroink H.²,Koenderink J. B.³,Kors E. E.⁴,van den Heuvel J. J. M. W.³,van den Boogerd E. H.¹,Stam A. H.⁴,Haan J.⁴⁵,De Vries B. B. A.⁶,Terwindt G. M.⁴,Frants R. R.¹,Ferrari M. D.⁴,van den Maagdenberg A. M. J. M.¹⁴

Affiliation:

1. Department of Human Genetics, Leiden University Medical Centre, Leiden

2. Department Neurology, St. Elisabeth and Tweesteden Hospital, Tilburg

3. Department Pharmacology and Toxicology, Nijmegen Centre for Molecular Life Sciences, Radboud University Nijmegen Medical Centre, Nijmegen

4. Department Neurology, Leiden University Medical Centre Leiden, Leiden

5. Department Neurology, Rijnland Hospital, Leiderdorp

6. Department Human Genetics, Radboud University Nijmegen Medical Centre, Nijmegen, The Netherlands

Funder

Netherlands Organization for Scientific Research

The Migraine Trust

EU “Eurohead”

Hersenstichting