Expanding the neuroimaging findings of guanidinoacetate methyltransferase deficiency in an Iranian girl with a homozygous frameshift variant in the GAMT.
Neurogenetics
; 24(2): 67-78, 2023 04.
Article
in En
| MEDLINE
| ID: mdl-36633690
Key words
Full text:
1
Collection:
01-internacional
Database:
MEDLINE
Main subject:
Language Development Disorders
/
Movement Disorders
Type of study:
Diagnostic_studies
/
Prognostic_studies
Limits:
Child
/
Female
/
Humans
/
Infant
Country/Region as subject:
Asia
Language:
En
Journal:
Neurogenetics
Journal subject:
GENETICA
/
NEUROLOGIA
Year:
2023
Type:
Article
Affiliation country:
United States