Skip to content
Open Access
  • Home
  • Collections
    • High Impact Articles
    • Jawi Collection
    • Malay Medicine
    • Forensic
  • Search Options
    • UiTM Open Access
    • Search by UiTM Scopus
    • Advanced Search
    • Search by Category
  • Discovery Service
    • Sources
    • UiTM Journals
    • List UiTM Journal in IR
    • Statistic
  • About
    • Open Access
    • Creative Commons Licenses
    • COKI | Malaysia Open Access
    • User Guide
    • Contact Us
    • Search Tips
    • FAQs
Advanced
  • PRRT2 gene mutations in Indian...
  • Cite this
  • Text this
  • Email this
  • Print
  • Export Record
    • Export to RefWorks
    • Export to EndNoteWeb
    • Export to EndNote
  • Permanent link
PRRT2 gene mutations in Indian paroxysmal kinesigenic dyskinesia patients

PRRT2 gene mutations in Indian paroxysmal kinesigenic dyskinesia patients

Bibliographic Details
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
  • Holdings
  • Description
  • Similar Items
  • Staff View

Internet

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)

© 2020 | Services hosted by the Perpustakaan Tun Abdul Razak, | Universiti Teknologi MARA | Disclaimer


Loading...