Congenital disorder of glycosylphosphatidylinositol (GPI)-anchor biosynthesis—The phenotype of two patients with novel mutations in the PIGN and PGAP2 genes
- 30 January 2016
- journal article
- case report
- Published by Elsevier BV in European Journal of Paediatric Neurology
- Vol. 20 (3), 462-473
- https://doi.org/10.1016/j.ejpn.2016.01.007
Abstract
No abstract availableKeywords
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