Intracortical inhibition of the motor cortex in Segawa disease (DYT5).

There is no author summary for this article yet. Authors can add summaries to their articles on ScienceOpen to make them more accessible to a non-specialist audience.

Abstract

Segawa disease (autosomal dominant guanosine triphosphate cyclohydrolase I [GTP-I] deficiency, DYT5) is a hereditary dopa-responsive generalized dystonia.

Related collections

Author and article information

Journal

Journal ID (iso-abbrev): Neurology

Title: Neurology

Publisher: Ovid Technologies (Wolters Kluwer Health)

ISSN (Electronic): 1526-632X

ISSN (Print): 0028-3878

Publication date (Electronic): Mar 27 2007

Volume: 68

Issue: 13

Affiliations

[1 ] Department of Neurology, University of Tokyo, 7-3-1 Hongo, Bunkyo-ku, Tokyo, 113-8655, Japan. hanajima-tky@umin.ac.jp

Article

Publisher Item ID: 68/13/1039

DOI: 10.1212/01.wnl.0000257816.92101.54

PubMed ID: 17389309

SO-VID: 2a3358c0-c29f-484c-9246-bd9affd68ef2

History

Data availability:

Comments

Comment on this article

scite_

Cited by 3

See all cited by