𝔖 Bobbio Scriptorium
✦   LIBER   ✦

Maroteaux-lamy disease (mucopolysaccharidosis VI), subtype A: Deficiency of a N-acetylgalactosamine-4-sulfatase

✍ Scribed by John F. O'Brien; Michael Cantz; Jürgen Spranger


Book ID
118309370
Publisher
Elsevier Science
Year
1974
Tongue
English
Weight
431 KB
Volume
60
Category
Article
ISSN
0006-291X

No coin nor oath required. For personal study only.


📜 SIMILAR VOLUMES


An N-acetylgalactosamine-4-sulfatase mut
✍ Tom Litjens; C. Phillip Morris; Evelyn F. Robertson; Christoph Peters; Kurt von 📂 Article 📅 1992 🏛 John Wiley and Sons 🌐 English ⚖ 496 KB

Maroteaux-Lamy syndrome (mucopolysaccharidosis type VI, MPS VI) is an autosomally inherited lysosomal storage disorder caused by a deficiency of N~acetylgalactosamine-4-sulfatase (EC 3.1.6.1; 4.sulfatase). In order to determine the gene defect in a clinically severe MPS VI patient, polymerase chain