Author:
Bonesteele Grant,Gargus J. Jay,Curtin Emily,Tang Mabel,Rosenbloom Barry,Kimonis Virginia
Funder
Lysosomal Storage Diseases
Subject
Endocrinology,Genetics,Molecular Biology
Reference29 articles.
1. Online Mendelian Inheritance in Man, OMIM®,2020
2. Gaucher disease types 1, 2, and 3: differential mutations of the acid beta-glucosidase active site identified with conduritol B epoxide derivatives and sphingosine;Grabowski;Am. J. Hum. Genet.,1985
3. Metabolism of glucocerebrosides II. Evidence of an enzymatic deficiency in Gaucher’s disease;Brady;Biochem. Biophys. Res. Commun.,1965
4. Gaucher disease: pathological mechanisms and modern management;Jmoudiak;Br. J. Haematol.,2005
5. Phenotype, diagnosis, and treatment of Gaucher’s disease;Grabowski;Lancet,2008
Cited by
5 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