Author:
Ankleshwaria Chitra,Mistri Mehul,Bavdekar Ashish,Muranjan Mamta,Dave Usha,Tamhankar Parag,Khanna Varun,Jasinge Eresha,Nampoothiri Sheela,Edayankara Kadangot Suresh,Sheth Frenny,Gupta Sarita,Sheth Jayesh
Publisher
Springer Science and Business Media LLC
Subject
Genetics(clinical),Genetics
Reference32 articles.
1. Sheth, J., Mistri, M., Sheth, F., Shah, R., Bavdekar, A., Godbole, K. et al. Burden of lysosomal storage disorders in india: experience of 387 affected children from a single diagnostic facility. JIMD Rep. 12, 51–63 (2014).
2. Beutler, E. & Grabowski, G. Gaucher Disease in The Metabolic and Molecular Bases of Inherited Disease (eds Scriver C. R., Beaudet A. L., Sly W. S., Vale D., 3635–3668 (McGraw-Hill: New York, NY, USA, 2001).
3. Zhao, H. & Grabowski, G. Gaucher disease: perspectives on a prototype lysosomal disease. Cell Mol. Life Sci. 59, 694–707 (2002).
4. Horowitz, M. & Zimran, A. Mutations causing Gaucher disease. Hum. Mutat. 3, 1–11 (1994).
5. Rozenberg, R., Fox, D., Sobreira, E. & Pereira, L. Detection of 12 new mutations in Gaucher disease Brazilian patients. Blood Cells Mol. Dis. 37, 204–209 (2006).
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