Long read sequencing characterises a novel structural variant, revealing underactive AKR1C1 with overactive AKR1C2 as a possible cause of severe chronic fatigue.
J Transl Med
; 21(1): 825, 2023 11 17.
Article
in En
| MEDLINE
| ID: mdl-37978513
Key words
Full text:
1
Collection:
01-internacional
Database:
MEDLINE
Main subject:
Fatigue Syndrome, Chronic
Limits:
Humans
Language:
En
Journal:
J Transl Med
Year:
2023
Type:
Article
Affiliation country:
United kingdom