Developmental disorder and spastic paraparesis in two sisters with a TCF7L2 truncating variant inherited from a mosaic mother.
Am J Med Genet A
; 191(6): 1658-1663, 2023 06.
Article
in En
| MEDLINE
| ID: mdl-36905089
Full text:
1
Collection:
01-internacional
Database:
MEDLINE
Main subject:
Spastic Paraplegia, Hereditary
/
Paraparesis, Spastic
Type of study:
Diagnostic_studies
Limits:
Child
/
Female
/
Humans
Language:
En
Journal:
Am J Med Genet A
Journal subject:
GENETICA MEDICA
Year:
2023
Type:
Article
Affiliation country:
Switzerland