home : about us : ahead of print : current issue : archives search instructions : subscriptionLogin 
Users online: 238      Small font sizeDefault font sizeIncrease font size Print this page Email this page
 LETTER TO THE EDITOR
Year : 2017  |  Volume : 12  |  Issue : 1  |  Page : 112-113

Proline-rich transmembrane protein 2 gene mutation in a sporadic paroxysmal kinesigenic dyskinesia


1 Division of Pediatric Neurology, Department of Neonatal, Pediatric and Adolescent Medicine, BLK Super Speciality Hospital, New Delhi; Division of Neurology, Department of Pediatrics, The Hospital for Sick Children, Toronto, Ontario, Canada, M5G1X8
2 Department of Pediatrics, Division of Pediatric Neurology, Lady Harding Medical College, Kalawati Saran Children Hospital, New Delhi, India
3 Department of Clinical Genetics, Erasmus MC, Rotterdam, The Netherlands

Correspondence Address:
Puneet Jain
Division of Neurology, Department of Pediatrics, The Hospital for Sick Children, Toronto, Ontario

Login to access the Email id

Source of Support: None, Conflict of Interest: None


DOI: 10.4103/jpn.JPN_148_16

Rights and Permissions








[FULL TEXT] [PDF]*


        
Print this article     Email this article
 Next article
 Previous article
 Table of Contents

 Similar in PUBMED
   Search Pubmed for
   Search in Google Scholar for
 Citation Manager
 Access Statistics
 Reader Comments
 Email Alert *
 Add to My List *
 * Requires registration (Free)
 

 Article Access Statistics
    Viewed1641    
    Printed32    
    Emailed0    
    PDF Downloaded44    
    Comments [Add]    

Recommend this journal