Genomic organization of the human phosphomannose isomerase (MPI) gene and mutation analysis in patients with congenital disorders of glycosylation type Ib (CDG-Ib)

✍ Scribed by E. Schollen; L. Dorland; T.J. de Koning; O.P. Van Diggelen; J.G.M. Huijmans; T. Marquardt; D. Babovic-Vuksanovic; M. Patterson; F. Imtiaz; B. Winchester; M. Adamowicz; E. Pronicka; H. Freeze; G. Matthijs

• Publisher: John Wiley and Sons
• Year: 2000
• Tongue: English
• Weight: 225 KB
• Volume: 16
• Category: Article
• ISSN: 1059-7794
• DOI: 10.1002/1098-1004(200009)16:3<247::aid-humu7>3.0.co;2-a

✦ Synopsis

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