Homozygous deletion of exon 18 leads to degradation of the lysosomal α-glucosidase precursor and to the infantile form of glycogen storage disease type II

✍ Scribed by Margreet G. E. M. Ausems; Marian A. Kroos; Magna Van der Kraan; Jan A. M. Smeitink; Wim J. Kleijer; Hans Kristian Ploos van Amstel; Arnold J. J. Reuser

• Book ID: 115091917
• Publisher: John Wiley and Sons
• Year: 2008
• Tongue: English
• Weight: 488 KB
• Volume: 49
• Category: Article
• ISSN: 0009-9163
• DOI: 10.1111/j.1399-0004.1996.tb03801.x