Functional characterization of two novel mutations in TTF-1/NKX2.1 homeodomain in patients with benign hereditary chorea.
J Neurol Sci
; 360: 78-83, 2016 Jan 15.
Article
in En
| MEDLINE
| ID: mdl-26723978
Key words
Full text:
1
Collection:
01-internacional
Database:
MEDLINE
Main subject:
Transcription Factors
/
Nuclear Proteins
/
Chorea
/
Mutation, Missense
Limits:
Adult
/
Child
/
Female
/
Humans
/
Male
Language:
En
Journal:
J Neurol Sci
Year:
2016
Document type:
Article
Affiliation country:
Italy