Depression, sleep disturbances, pain, disability and quality of LIFE in Brazilian Fabry disease patients

Background: Fabry disease (FD) is a lysosomal disease in which mutations affect the GLA gene located on the X chromosome. The defective product, the enzyme alpha-galactosidase A, causes accumulation of substrate and contributes to the disruption of cell function in several organs, with variable seve...

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Detalles Bibliográficos
Autores principales: Rosa Neto, Nilton Salles, Bento, Judith Campos de Barros, Pereira, Rosa Maria Rodrigues
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Elsevier 2019
Materias:
Research Paper
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6909105/
https://www.ncbi.nlm.nih.gov/pubmed/31871893
http://dx.doi.org/10.1016/j.ymgmr.2019.100547

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6909105/
https://www.ncbi.nlm.nih.gov/pubmed/31871893
http://dx.doi.org/10.1016/j.ymgmr.2019.100547

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