Clinical and genetic characterization of a Chinese family with pontocerebellar hypoplasia type 7.
Am J Med Genet A
; 194(1): 46-52, 2024 Jan.
Article
in En
| MEDLINE
| ID: mdl-37608778
Key words
Full text:
1
Collection:
01-internacional
Database:
MEDLINE
Main subject:
Cerebellar Diseases
/
Intellectual Disability
Type of study:
Prognostic_studies
Limits:
Female
/
Humans
/
Male
Country/Region as subject:
Asia
Language:
En
Journal:
Am J Med Genet A
Journal subject:
GENETICA MEDICA
Year:
2024
Type:
Article
Affiliation country:
China