PRRT2c.649dupC Mutation Derived fromDe Novoin Paroxysmal Kinesigenic Dyskinesia-Reference-Cited by-同舟云学术

PRRT2c.649dupC Mutation Derived fromDe Novoin Paroxysmal Kinesigenic Dyskinesia

Published:2012-11-24 Issue:1 Volume:19 Page:61-65
ISSN:1755-5930
Container-title:CNS Neuroscience & Therapeutics
language:en
Short-container-title:CNS Neurosci Ther

Author:

Li Hong-Fu¹,Ni Wang¹,Xiong Zhi-Qi²,Xu Jianfeng³,Wu Zhi-Ying¹

Affiliation:

1. Department of Neurology and Institute of Neurology; Huashan Hospital; Institutes of Brain Science and State Key Laboratory of Medical Neurobiology; Shanghai Medical College; Fudan University; Shanghai; China

2. Institute of Neuroscience; State Key Laboratory of Neuroscience; Shanghai Institutes for Biological Sciences; Chinese Academy of Sciences; Shanghai; China

3. Fudan-VARI Center for Genetic Epidemiology; School of Life Science; Fudan University; Shanghai; China

Publisher

Wiley

Subject

Pharmacology (medical),Physiology (medical),Psychiatry and Mental health,Pharmacology

Link

http://onlinelibrary.wiley.com/wol1/doi/10.1111/cns.12034/fullpdf

Reference17 articles.

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2. Paroxysmal kinesigenic choreoathetosis: A report of 26 patients;Houser;J Neurol,1999

3. Paroxysmal dyskinesias: Clinical features and classification;Demirkiran;Ann Neurol,1995

4. Familial infantile convulsions and paroxysmal choreoathetosis: A new neurological syndrome linked to the pericentromeric region of human chromosome 16;Szepetowski;Am J Hum Genet,1997

5. Linkage of benign familial infantile convulsions to chromosome 16p12-q12 suggests allelism to the infantile convulsions and choreoathetosis syndrome;Caraballo;Am J Hum Genet,2001

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