Comprehensive and differential long-term characterization of the alpha-galactosidase A deficient mouse model of Fabry disease focusing on the sensory system and pain development

BACKGROUND: Fabry disease is an X-linked lysosomal storage disorder due to impaired activity of alpha-galactosidase A with intracellular accumulation of globotriaosylceramide. Associated small fiber pathology leads to characteristic pain in Fabry disease. We systematically assessed sensory system, p...

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Detalles Bibliográficos
Autores principales: Üçeyler, Nurcan, Biko, Lydia, Hose, Dorothea, Hofmann, Lukas, Sommer, Claudia
Formato: Online Artículo Texto
Lenguaje:English
Publicado: SAGE Publications 2016
Materias:
Research Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4956180/
https://www.ncbi.nlm.nih.gov/pubmed/27145802
http://dx.doi.org/10.1177/1744806916646379

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4956180/
https://www.ncbi.nlm.nih.gov/pubmed/27145802
http://dx.doi.org/10.1177/1744806916646379

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