Defects of mutant DNMT1 are linked to a spectrum of neurological disorders.
Brain
; 138(Pt 4): 845-61, 2015 Apr.
Article
in En
| MEDLINE
| ID: mdl-25678562
Key words
Full text:
1
Collection:
01-internacional
Database:
MEDLINE
Main subject:
Hereditary Sensory and Autonomic Neuropathies
/
DNA (Cytosine-5-)-Methyltransferases
/
Mutation
Type of study:
Diagnostic_studies
/
Prognostic_studies
Limits:
Adult
/
Aged
/
Female
/
Humans
/
Male
/
Middle aged
Language:
En
Journal:
Brain
Year:
2015
Document type:
Article
Affiliation country:
Belgium
Country of publication:
United kingdom