A new tyrosine hydroxylase genotype associated with early-onset severe encephalopathy.
J Child Neurol
; 27(4): 523-5, 2012 Apr.
Article
in En
| MEDLINE
| ID: mdl-21940685
Full text:
1
Collection:
01-internacional
Database:
MEDLINE
Main subject:
Psychomotor Disorders
/
Tyrosine 3-Monooxygenase
/
Mutation, Missense
Type of study:
Prognostic_studies
/
Risk_factors_studies
Limits:
Child, preschool
/
Humans
/
Male
Language:
En
Journal:
J Child Neurol
Journal subject:
NEUROLOGIA
/
PEDIATRIA
Year:
2012
Document type:
Article
Affiliation country:
Italy