Identification of novel CSNK2A1 variants and the genotype-phenotype relationship in patients with Okur-Chung neurodevelopmental syndrome: a case report and systematic literature review.
J Int Med Res
; 49(5): 3000605211017063, 2021 May.
Article
in En
| MEDLINE
| ID: mdl-34038195
Key words
Full text:
1
Collection:
01-internacional
Database:
MEDLINE
Main subject:
Neurodevelopmental Disorders
/
Intellectual Disability
Type of study:
Diagnostic_studies
/
Prognostic_studies
/
Systematic_reviews
Limits:
Child
/
Humans
Language:
En
Journal:
J Int Med Res
Year:
2021
Document type:
Article
Country of publication:
United kingdom