Funder
Indian Council of Medical Research and Department of Heath Research,Govt of India
Publisher
Springer Science and Business Media LLC
Subject
Genetics (clinical),Genetics
Reference11 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. 2014;12:51–63.
2. Gravel RA, Kaback MM, Proia RL, Sandhoff K, Suzuki K. The GM2 gangliosidosis. In: Scriver CR, Beaudet AL, Sly WS, Valle D, editors. The metabolic and molecular bases of inherited disease. New York: McGraw-Hill; 1995. p. 3827–76.
3. Sonnino S, Chigorno V. Ganglioside molecular species containing C18- and C20-sphingosine in mammalian nervous tissues and neuronal cell cultures. Biochim Biophys Acta. 2000;1469:63–77.
4. Proia L, Neufeld EF. Synthesis of beta-hexosaminidase in cell-free translation and in intact fibroblasts: an insoluble precursor alpha chain in a rare form of Tay-Sachs disease. Proc Nat Acad Sci. 1982;79:6360–4.
5. Myerowitz R, Hogikyan ND. Different mutations in Ashkenazi Jewish and non-Jewish French Canadians with Tay-Sachs disease. Science. 1986;232(4758):1646–8.
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