A new mutation (Thr106Ile) of the GTP cyclohydrolase 1 gene associated with DYT5 dystonia (Segawa disease)

Saved in:
Bibliographic Details
Published in:Movement disorders 2005-08, Vol.20 (8), p.1083-1084
Main Authors: Ohta, Etsuro, Toyoshima, Itaru, Funayama, Manabu, Ichinose, Hiroshi, Hasegawa, Kazuko, Obata, Fumiya
Format: Article
Language:English
Subjects:
Adult
Child
DNA Mutational Analysis - methods
Dystonic Disorders - genetics
Exons
Female
GTP Cyclohydrolase - genetics
Humans
Isoleucine - genetics
Mutation
Threonine - genetics
Citations: Items that this one cites
Items that cite this one
Online Access:Get full text
Tags: Add Tag
No Tags, Be the first to tag this record!
Description
Summary:
ISSN:0885-3185
1531-8257
DOI:10.1002/mds.20490