Altered immune phenotypes in subjects with Fabry disease and responses to switching from agalsidase alfa to agalsidase beta

Fabry disease (FD) is a rare X-linked genetic disorder caused by mutations in the GLA gene encoding the lysosomal enzyme, α-galactosidase A (α-gal A). The mutations lead to lack of or faulty enzyme causing accumulation of globotriaosylceramide (Gb3) and related glycosphingolipids including globotria...

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Detalhes bibliográficos
Publicado no:Am J Transl Res
Main Authors: Limgala, Renuka P, Jennelle, Tabitha, Plassmeyer, Matthew, Boutin, Michel, Lavoie, Pamela, Abaoui, Mona, Auray-Blais, Christiane, Nedd, Khan, Alpan, Oral, Goker-Alpan, Ozlem
Formato: Artigo
Idioma:Inglês
Publicado em: e-Century Publishing Corporation 2019
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Original Article
Acesso em linha:https://ncbi.nlm.nih.gov/pmc/articles/PMC6456521/
https://ncbi.nlm.nih.gov/pubmed/30972193
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