|1.||Al-Hassnan, Zuhair: 1 article (10/2008)|
|2.||Al-Aqeel, Aida I: 1 article (10/2008)|
|3.||Awartani, Khalid: 1 article (10/2008)|
|4.||Qubbaj, Wafa: 1 article (10/2008)|
|5.||Coskun, Serdar: 1 article (10/2008)|
|6.||Al-Rejjal, Rafat: 1 article (10/2008)|
|7.||Al-Duraihim, Adel: 1 article (10/2008)|
|1.||Mucopolysaccharidosis IV (Morquio Syndrome)
10/01/2008 - "Morquio syndrome is an autosomal recessive disease and mutations in the N-acetylgalactosamine 6-sulfate sulfatase (GALNS) gene cause Morquio type A disease. "
07/01/1982 - "Using this substrate, we found there was a striking deficiency of galactose 6-sulfate sulfatase activity, in addition to the known deficiency of N-acetylgalactosamine 6-sulfate sulfatase, in the cultured skin fibroblasts of patients with Morquio syndrome. "
07/01/1982 - "Our results could be explained by the hypothesis that accumulation of keratan sulfate and chondroitin 6-sulfate in Morquio syndrome is due to a deficiency of galactose 6-sulfate sulfatase and N-acetylgalactosamine 6-sulfate sulfatase activity, which are necessary for the degradation of these two mucopolysaccharides."
|3.||Chondroitin Sulfates (Chondroitin Sulfate)