Non-coding CGG repeat expansion in LOC642361/NUTM2B-AS1 is associated with a phenotype of oculopharyngodistal myopathy.
J Med Genet
; 61(4): 340-346, 2024 Mar 21.
Article
in En
| MEDLINE
| ID: mdl-37923380
Full text:
1
Collection:
01-internacional
Database:
MEDLINE
Main subject:
Muscular Dystrophies
Limits:
Adult
/
Humans
Language:
En
Journal:
J Med Genet
Year:
2024
Document type:
Article
Affiliation country:
China
Country of publication:
Reino Unido