Heterozygous Deletion of KLHL1/ATX8OS at the SCA8 Locus Is Unlikely Associated With Cerebellar Impairment in Humans.

Subjects

Subjects :

Child
Female
Genetic Loci
Humans
Microfilament Proteins deficiency
Pedigree
Spinocerebellar Ataxias diagnosis
Cerebellum physiopathology
Genetic Predisposition to Disease
Heterozygote
Microfilament Proteins metabolism
Spinocerebellar Ataxias physiopathology

Details

Language :

English

ISSN :

1473-4230

Volume :

15

Issue :

2

Database :

MEDLINE

Journal :

Cerebellum (London, England)

Publication Type :

Academic Journal

Accession number :

25998497

Full Text :

https://doi.org/10.1007/s12311-015-0679-3