Genomic organization of the human phosphomannose isomerase (MPI) gene and mutation analysis in patients with congenital disorders of glycosylation type Ib (CDG-Ib)
Els Schollen(KU Leuven), Gert Matthijs(VIB-KU Leuven Center for Cancer Biology), Tom J. de Koning(University Medical Center Utrecht), Michael S. Adamowicz(Children's Memorial Health Institute), Faiqa Imtiaz(King Faisal Specialist Hospital & Research Centre), Ewa Pronicka(Children's Memorial Health Institute), Marc C. Patterson(Mayo Clinic), Dusica Babovic‐Vuksanovic(Mayo Clinic), Thorsten Marquardt(Klinik und Poliklinik für Kinder- und Jugendmedizin), L. Dorland(Uniwersytecki Szpital Dziecięcy), Bryan Winchester(Great Ormond Street Hospital), Hudson H. Freeze(Discovery Institute), O. P. van Diggelen(Erasmus MC), J. G. M. Huijmans(Erasmus MC)
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