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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.
- Source :
- Journal of Inherited Metabolic Disease Reports; Sep2020, Vol. 55 Issue 1, p38-43, 6p
- Publication Year :
- 2020
Details
- Language :
- English
- ISSN :
- 21928312
- Volume :
- 55
- Issue :
- 1
- Database :
- Complementary Index
- Journal :
- Journal of Inherited Metabolic Disease Reports
- Publication Type :
- Academic Journal
- Accession number :
- 145430360
- Full Text :
- https://doi.org/10.1002/jmd2.12149