LETTER TO THE EDITOR |
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Year : 2017 | Volume
: 12
| Issue : 1 | Page : 112-113 |
Proline-rich transmembrane protein 2 gene mutation in a sporadic paroxysmal kinesigenic dyskinesia
Puneet Jain1, Suvasini Sharma2, Guido Breedveld3, Vincenzo Bonifati3, Satinder Aneja2
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  | Check |
DOI: 10.4103/jpn.JPN_148_16
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