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Genomic organization of the human phosphomannose isomerase (MPI) gene and mutation analysis in patients with congenital disorders of glycosylation type Ib (CDG-Ib).
E Schollen, L Dorland, T J de Koning, O P Van Diggelen, J G Huijmans, T Marquardt, D Babovic-Vuksanovic, M Patterson, F Imtiaz, B Winchester, M Adamowicz, E Pronicka, H Freeze, G Matthijs
Human Mutation 2000; 16(3):247-252
ICID: 740585
IC™ Value: 7.53
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