Codon 101 of PRKCG, a preferential mutation site in SCA14.

Subjects

Subjects :

DNA Mutational Analysis
Exons genetics
Family Health
Histidine genetics
Humans
Male
Middle Aged
Spinocerebellar Ataxias classification
Tyrosine genetics
Codon genetics
Mutation
Protein Kinase C genetics
Spinocerebellar Ataxias genetics

Details

Language :

English

ISSN :

0885-3185

Volume :

22

Issue :

12

Database :

MEDLINE

Journal :

Movement disorders : official journal of the Movement Disorder Society

Publication Type :

Report

Accession number :

17659643

Full Text :

https://doi.org/10.1002/mds.21654