Back to Search Start Over

SPG46 due to truncating mutations in GBA2: Two cases from India.

Authors :
Holla VV
Surisetti BK
Prasad S
Thota N
Stezin A
Pal PK
Yadav R
Source :
Parkinsonism & related disorders [Parkinsonism Relat Disord] 2021 Jan; Vol. 82, pp. 13-15. Date of Electronic Publication: 2020 Nov 17.
Publication Year :
2021

Subjects

Subjects :
Adult
Consanguinity
Dystonia etiology
Dystonia physiopathology
Female
Head Movements physiology
Humans
India
Male
Pedigree
Spastic Paraplegia, Hereditary complications
Spastic Paraplegia, Hereditary diagnosis
Tremor etiology
Tremor physiopathology
Young Adult
Glucosylceramidase genetics
Spastic Paraplegia, Hereditary genetics
Spastic Paraplegia, Hereditary physiopathology

Details

Language :
English
ISSN :
1873-5126
Volume :
82
Database :
MEDLINE
Journal :
Parkinsonism & related disorders
Publication Type :
Report
Accession number :
33227682
Full Text :
https://doi.org/10.1016/j.parkreldis.2020.11.007
Full Text Access
View/download PDF

Tools

Authors Abstract Subjects Details