GRIN2B encephalopathy: novel findings on phenotype, variant clustering, functional consequences and treatment aspects.
J Med Genet
; 54(7): 460-470, 2017 07.
Article
in En
| MEDLINE
| ID: mdl-28377535
Key words
Full text:
1
Collection:
01-internacional
Database:
MEDLINE
Main subject:
Brain Diseases
/
Receptors, N-Methyl-D-Aspartate
/
Mutation
Type of study:
Diagnostic_studies
Limits:
Humans
Language:
En
Journal:
J Med Genet
Year:
2017
Document type:
Article
Affiliation country:
Alemania
Country of publication:
Reino Unido