Molecular analysis of the iduronate-2-sulfatase gene in Thai patients with Hunter syndrome

• المؤلفون الرئيسيون: Keeratichamroen S., Ketudat Cairns J.R., Wattanasirichaigoon D., Wasant P., Ngiwsara L., Suwannarat P., Pangkanon S., Kuptanon J., Tanpaiboon P., Rujirawat T., Liammongkolkul S., Svasti J.
• التنسيق: مقال
• اللغة: English
• منشور في: Springer Netherlands 2014
• الوصول للمادة أونلاين: http://www.scopus.com/inward/record.url?eid=2-s2.0-43949121459&partnerID=40&md5=bef966cddae50340cc35284c98c9b2a3; http://cmuir.cmu.ac.th/handle/6653943832/2428

Molecular defects in the gene encoding the enzyme iduronate-2-sulfatase (IDS) result in Hunter disease (mucopolysaccharidosis type II, MPS II). To determine the molecular basis of MPS II in Thailand, the IDS gene was analysed in 20 Thai patients with Hunter syndrome from 18 unrelated families. A tot...