Biallelic variants in PAX3 cause Klein syndrome.
Clin Genet
; 102(3): 223-227, 2022 09.
Article
in En
| MEDLINE
| ID: mdl-35607853
Key words
Full text:
1
Collection:
01-internacional
Database:
MEDLINE
Main subject:
Waardenburg Syndrome
/
PAX3 Transcription Factor
Type of study:
Diagnostic_studies
Limits:
Child
/
Humans
Language:
En
Journal:
Clin Genet
Year:
2022
Document type:
Article
Affiliation country:
Country of publication: