Author:
Young-Gqamana Brandy,Brignol Nastry,Chang Hui-Hwa,Khanna Richie,Soska Rebecca,Fuller Maria,Sitaraman Sheela A.,Germain Dominique P.,Giugliani Roberto,Hughes Derralynn A.,Mehta Atul,Nicholls Kathy,Boudes Pol,Lockhart David J.,Valenzano Kenneth J.,Benjamin Elfrida R.
Publisher
Public Library of Science (PLoS)
Reference53 articles.
1. Desnick R, Ioannou Y, Eng C (2001) α-Galactosidase A deficiency: Fabry disease. In: Scriver C, Beaudet A, Sly W, Valle D, editors. The Metabolic and Molecular Bases of Inherited Disease. New York, New York, USA: McGraw-Hill. 3733–3774.
2. Cellular and tissue localization of globotriaosylceramide in Fabry disease;H Askari;Virchows Arch,2007
3. Enzymatic defect in Fabry's disease: ceramide trihexosidase deficiency;OR Brady;N Engl J Med,1967
4. Fabry's disease: classification as a sphingolipidosis and partial characterization of a novel glycolipid;CC Sweeley;J Biol Chem,1963
5. Germain DP (2010) Fabry disease. Orphanet J Rare Dis doi:10.1186/1750-1172-5-30.
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