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Rare Variant of GM2 Gangliosidosis through Activator-Protein Deficiency

Florian Brackmann1, Christiane Kehrer2, Wibke Kustermann1

  • 1Division of Neuropediatrics, Department of Pediatrics, University Hospital Erlangen, Erlangen, Germany.

Neuropediatrics
|February 14, 2017
PubMed

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