Abnormalities of motor function, transcription and cerebellar structure in mouse models of THAP1 dystonia.

Ruiz, Marta

Abnormalities of motor function, transcription and cerebellar structure in mouse models of THAP1 dystonia. [electronic resource] - Human molecular genetics Dec 2015 - 7159-70 p. digital

Publication Type: Journal Article; Research Support, N.I.H., Extramural; Research Support, Non-U.S. Gov't

1460-2083

10.1093/hmg/ddv384 doi


Animals
Cerebellum--metabolism
DNA-Binding Proteins--genetics
Dystonia Musculorum Deformans--metabolism
Male
Mice
Mice, Mutant Strains
Mutation
RNA, Messenger--genetics