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

Puneet Jain¹, Suvasini Sharma², Guido Breedveld³, Vincenzo Bonifati³, Satinder Aneja^2
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

Source of Support: None, Conflict of Interest: None

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DOI: 10.4103/jpn.JPN_148_16