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Mild Clinical and Biochemical Phenotype in Two Patients with PMM2-CDG (Congenital Disorder of Glycosylation Ia)
M. Casado, M. M. O’Callaghan, R. Montero, C. Pérez-Cerda, B. Pérez, P. Briones, E. Quintana, J. Muchart, A. Aracil, M. Pineda, R. ArtuchVolume:
11
Language:
english
Pages:
7
DOI:
10.1007/s12311-011-0313-y
Date:
June, 2012
File:
PDF, 343 KB
english, 2012