Mannose phosphate isomerase deficiency-congenital disorder of glycosylation (MPI-CDG) with cerebral venous sinus thrombosis as first and only presenting symptom: A rare but treatable cause of thrombophilia.
JIMD Rep
; 55(1): 38-43, 2020 Sep.
Article
en En
| MEDLINE
| ID: mdl-32905087
Texto completo:
1
Colección:
01-internacional
Base de datos:
MEDLINE
Tipo de estudio:
Diagnostic_studies
/
Prognostic_studies
Idioma:
En
Revista:
JIMD Rep
Año:
2020
Tipo del documento:
Article