๐”– Bobbio Scriptorium
โœฆ   LIBER   โœฆ

Polymorphisms in Tunisian patients with N-acetylgalactosamine-6-sulfate sulfatase gene deficiency: Implication in Morquio A disease

โœ Scribed by Souhir Khedhiri; Latifa Chkioua; Salima Ferchichi; Abdelhedi Miled; Sandrine Laradi


Book ID
115022885
Publisher
BioMed Central
Year
2011
Tongue
English
Weight
188 KB
Volume
6
Category
Article
ISSN
1746-1596

No coin nor oath required. For personal study only.


๐Ÿ“œ SIMILAR VOLUMES


Molecular analysis of Turkish mucopolysa
โœ Mugen Terzioglu; Aysegul Tokatli; Turgay Coskun; Serap Emre ๐Ÿ“‚ Article ๐Ÿ“… 2002 ๐Ÿ› John Wiley and Sons ๐ŸŒ English โš– 40 KB ๐Ÿ‘ 2 views

Mucopolysaccharidosis IVA (MPS IVA) is a lysosomal storage disorder caused by the deficiency of N-acetylgalactosamine-6-sulfate sulfatase (GALNS; EC 3.1.6.4). The deficiency of N-acetylgalactosamine-6-sulfate sulfatase leads to lysosomal accumulation of undegraded glycosaminoglycans, keratan sulfate