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

Overview of attention for article published in Orphanet Journal of Rare Diseases, September 2017

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Biblioteca Digital de l'Hospital Universitari Vall d'Hebron. ICS, 18 Sep 2017

A quantitative assessment of the evolution of cerebellar syndrome https://t.co/pZB5CTPDcC #hvhebron #neuroped [Text complet] @ojr…

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