Rituximab to treat prolidase deficiency due to a novel pathogenic copy number variation in PEPD.
RMD Open
; 9(4)2023 Dec 07.
Article
in En
| MEDLINE
| ID: mdl-38088248
Full text:
1
Database:
MEDLINE
Main subject:
Sjogren's Syndrome
/
Prolidase Deficiency
Limits:
Adult
/
Child
/
Female
/
Humans
Language:
En
Journal:
RMD Open
Year:
2023
Type:
Article
Affiliation country:
Germany