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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.

Authors :
Mühlhausen, Chris
Henneke, Lisa
Schlotawa, Lars
Behme, Daniel
Grüneberg, Marianne
Gärtner, Jutta
Marquardt, Thorsten
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