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
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