Author:
Harmanci Ozgur,Bayraktar Yusuf
Publisher
Baishideng Publishing Group Inc.
Subject
Gastroenterology,General Medicine
Reference55 articles.
1. Scriver CR, Beaudet AL, Valle D, Sly WS. The metabolic and molecular basis of inherited disease. 8th ed New York: McGraw-Hill Pub; 2001;3635-3668.
2. Schnabel D, Schroder M, Sandhoff K. Mutation in the sphingolipid activator protein 2 in a patient with a variant of Gaucher disease. FEBS Lett 1991;284:57-69.
3. Gurakan F, Terzioglu M, Kocak N, Yuce A, Ozen H, Ciliv G, Emre S. Analysis of three mutations in Turkish children with Gaucher disease. J Inherit Metab Dis 1999;22:947-948.
4. Eto Y, Ida H. Clinical and molecular characteristics of Japanese Gaucher disease. Neurochem Res 1999;24:207-211.
5. Wan L, Hsu CM, Tsai CH, Lee CC, Hwu WL, Tsai FJ. Mutation analysis of Gaucher disease patients in Taiwan: high prevalence of the RecNciI and L444P mutations. Blood Cells Mol Dis 2006;36:422-425.
Cited by
25 articles.
订阅此论文施引文献
订阅此论文施引文献，注册后可以免费订阅5篇论文的施引文献，订阅后可以查看论文全部施引文献