Lyso-glycosphingolipid abnormalities in different murine models of lysosomal storage disorders

Author:

Ferraz Maria J.,Marques André R.A.,Gaspar Paulo,Mirzaian Mina,van Roomen Cindy,Ottenhoff Roelof,Alfonso Pilar,Irún Pilar,Giraldo Pilar,Wisse Patrick,Sá Miranda Clara,Overkleeft Herman S.,Aerts Johannes M.

Funder

ERC AdG CHEMBIOSPHIN

Fundação para a Ciência e Tecnologia

Publisher

Elsevier BV

Subject

Endocrinology,Genetics,Molecular Biology,Biochemistry,Endocrinology, Diabetes and Metabolism

Reference60 articles.

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3. Niemann–Pick C1 disease gene: homology to mediators of cholesterol homeostasis;Carstea;Science,1997

4. Identification of HE1 as the second gene of Niemann–Pick C disease;Naureckiene;Science,2000

5. Additional deficiency of psychosine galactosidase in globoid cell leukodystrophy: an implication to enzyme replacement therapy;Miyatake;Birth Defects Orig. Artic. Ser.,1973

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