PRRT2 gene mutations in Indian paroxysmal kinesigenic dyskinesia patients
Main Authors: | S Prabhakara, H M Hanumantha Rao, L K Prashanth, K Anbazhagan, Rochette Jacques, Basanth Kumar Reddy |
---|---|
Format: | Article |
Language: | English |
Published: |
Wolters Kluwer Medknow Publications
2021-01-01
|
Series: | Annals of Indian Academy of Neurology |
Online Access: | http://www.annalsofian.org/article.asp?issn=0972-2327;year=2021;volume=24;issue=3;spage=425;epage=429;aulast=Prabhakara |
Similar Items
-
Molecular analysis of PRRT2 gene in a case of paroxysmal kinesigenic dyskinesia patient
by: S Prabhakara, et al.
Published: (2014-01-01) -
Mutations in the Gene PRRT2 Cause Paroxysmal Kinesigenic Dyskinesia with Infantile Convulsions
by: Hsien-Yang Lee, et al.
Published: (2012-01-01) -
Novel <it>PRRT2</it> mutation in an African-American family with paroxysmal kinesigenic dyskinesia
by: Hedera Peter, et al.
Published: (2012-09-01) -
PRRT2 mutations in paroxysmal kinesigenic dyskinesia with infantile convulsions in a Taiwanese cohort.
by: Yi-Chung Lee, et al.
Published: (2012-01-01) -
Characterization of pathomechanisms of PRRT2 mutations involving Paroxysmal kinesigenic dyskinesia and its related neurological disorders
by: Fang-Shin Nian, et al.
Published: (2019)