A de novo SCA14 mutation in an isolated case of late-onset cerebellar ataxia.

van Gaalen, Judith

A de novo SCA14 mutation in an isolated case of late-onset cerebellar ataxia. [electronic resource] - Movement disorders : official journal of the Movement Disorder Society Nov 2013 - 1902-3 p. digital

Publication Type: Case Reports; Letter

1531-8257

10.1002/mds.25572 doi


Humans
Male
Middle Aged
Protein Kinase C--genetics
Spinocerebellar Ataxias
Spinocerebellar Degenerations--genetics