De novo variants in RNF213 are associated with a clinical spectrum ranging from Leigh syndrome to early-onset stroke.
Genet Med
; 26(2): 101013, 2024 Feb.
Article
in En
| MEDLINE
| ID: mdl-37924258
Full text:
1
Collection:
01-internacional
Database:
MEDLINE
Main subject:
Leigh Disease
/
Stroke
/
Moyamoya Disease
Limits:
Child
/
Humans
Language:
En
Journal:
Genet Med
Journal subject:
GENETICA MEDICA
Year:
2024
Type:
Article