TY  - GEN
AU  - Stevanin,Giovanni
AU  - Hahn,Valérie
AU  - Lohmann,Ebba
AU  - Bouslam,Naima
AU  - Gouttard,Michel
AU  - Soumphonphakdy,Caroline
AU  - Welter,Marie-Laure
AU  - Ollagnon-Roman,Elisabeth
AU  - Lemainque,Arnaud
AU  - Ruberg,Merle
AU  - Brice,Alexis
AU  - Durr,Alexandra
TI  - Mutation in the catalytic domain of protein kinase C gamma and extension of the phenotype associated with spinocerebellar ataxia type 14
SN  - 0003-9942
PY  - 2004///0907
KW  - Adult
KW  - Aged
KW  - Amino Acid Sequence
KW  - Base Sequence
KW  - Brain
KW  - pathology
KW  - Catalytic Domain
KW  - genetics
KW  - Chromosomes, Human, Pair 19
KW  - enzymology
KW  - Female
KW  - Genetic Linkage
KW  - Humans
KW  - Male
KW  - Middle Aged
KW  - Molecular Sequence Data
KW  - Mutation, Missense
KW  - Pedigree
KW  - Phenotype
KW  - Protein Kinase C
KW  - Spinocerebellar Ataxias
N1  - Publication Type: Journal Article; Research Support, Non-U.S. Gov't
UR  - https://doi.org/10.1001/archneur.61.8.1242
ER  -