Refining the mutational spectrum and gene-phenotype correlates in pontocerebellar hypoplasia: results of a multicentric study.
J Med Genet
; 59(4): 399-409, 2022 04.
Article
in En
| MEDLINE
| ID: mdl-34085948
Key words
Full text:
1
Collection:
01-internacional
Database:
MEDLINE
Main subject:
Olivopontocerebellar Atrophies
/
Cerebellar Diseases
Type of study:
Clinical_trials
/
Diagnostic_studies
Limits:
Female
/
Humans
/
Male
Language:
En
Journal:
J Med Genet
Year:
2022
Document type:
Article
Affiliation country:
Italia
Country of publication:
Reino Unido