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Elsevier, European Journal of Paediatric Neurology

DOI: 10.1016/j.ejpn.2016.01.007

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Congenital disorder of glycosylphosphatidylinositol (GPI)-anchor biosynthesis-The phenotype of two patients with novel mutations in the PIGN and PGAP2 genes

This paper is available in a repository.
This paper is available in a repository.

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