𝔖 Bobbio Scriptorium
✦   LIBER   ✦

Glucose-Containing Oligosaccharides in the Urine of Patients with Glycogen Storage Disease Type II and Type III

✍ Scribed by Gudrun LENNARTSON; Arne LUNDBLAD; Jörgen LUNDSTEN; Sigfrid SVENSSON; Anders HÄGER


Book ID
115116485
Publisher
John Wiley and Sons
Year
1978
Tongue
English
Weight
634 KB
Volume
83
Category
Article
ISSN
1432-1327

No coin nor oath required. For personal study only.


📜 SIMILAR VOLUMES


Novel mutations in African American pati
✍ Nina Raben; Eunice Lee; Laura Lee; Rochelle Hirschhorn; Paul H. Plotz 📂 Article 📅 1999 🏛 John Wiley and Sons 🌐 English ⚖ 74 KB 👁 1 views

The infantile form of GSD II (an inherited deficiency of the lysosomal enzyme, acid α αglucosidase, Pompe disease) is a severe and invariably fatal disease characterized by a rapidly progressive generalized hypotonia, hepatomegaly, and cardiomegaly. We have recently demonstrated that African America