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Additional file 2: of A quantitative assessment of the evolution of cerebellar syndrome in children with phosphomannomutase-deficiency (PMM2-CDG)

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posted on 2017-09-15, 05:00 authored by Natalia Serrano, Victor De Diego, Daniel Cuadras, Antonio Martinez Monseny, Ramón Velázquez-Fragua, Laura López, Ana Felipe, Luis Gutiérrez-Solana, Alfons Macaya, Belén Pérez-Dueñas, Mercedes Serrano
Cerebellar volumetric study, molecular and clinical characteristics of Patients 3, 5 and 7. (TIFF 3555 kb)

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    Orphanet Journal of Rare Diseases

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