Stroke and Fabry Disease: A Review of Literature

Fabry disease is an X-linked lysosomal storage disorder caused by a mutation in the alpha-galactosidase A (GLA) gene, leading to the deficiency of alpha-galactosidase A enzyme. The natural history of the affected patients (both males and females) includes neurovascular complications, such as cerebro...

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Dades bibliogràfiques
Publicat a:Cureus
Autors principals: Mishra, Vinayak, Banerjee, Amit, Gandhi, Arohi B, Kaleem, Ifrah, Alexander, Josh, Hisbulla, Mohamed, Kannichamy, Vishmita, Valaiyaduppu Subas, Sharathshiva, Hamid, Pousette
Format: Artigo
Idioma:Inglês
Publicat: Cureus 2020
Matèries:
Genetics
Accés en línia:https://ncbi.nlm.nih.gov/pmc/articles/PMC7805529/
https://ncbi.nlm.nih.gov/pubmed/33489501
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.7759/cureus.12083
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