CSF N-glycan profile reveals sialylation deficiency in a patient with GM2 gangliosidosis presenting as childhood disintegrative disorder-Reference-Cited by-同舟云学术

CSF N-glycan profile reveals sialylation deficiency in a patient with GM2 gangliosidosis presenting as childhood disintegrative disorder

Author:

Barone Rita¹,Sturiale Luisella²,Fiumara Agata³,Palmigiano Angelo²,Bua Rosaria O.²,Rizzo Renata¹,Zappia Mario⁴,Garozzo Domenico²

Affiliation:

1. Child Neurology and Psychiatry Unit, Department of Clinical and Experimental Medicine, University of Catania

2. CNR-Institute for Polymers, Composites and Biomaterials IPCB; Catania

3. Centre for Inherited Metabolic Diseases, Department of Clinical and Experimental Medicine, University of Catania

4. Section of Neuroscience Department GF Ingrassia, University of Catania; Catania Italy

Publisher

Wiley

Subject

Genetics (clinical),Neurology (clinical),General Neuroscience

Reference28 articles.

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