Prevalence of antibodies to ganglioside and Hep 2 in Gaucher, Niemann – Pick type C and Sanfilippo diseases

Lysosomal Storage Diseases (LSDs) are rare genetic diseases, the majority of which are caused by specific lysosomal enzyme deficiencies and all are characterized by malfunctioning lysosomes. Lysosomes are key regulators of many different cellular processes and are vital for the function of the immun...

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Detalles Bibliográficos
Autores principales: Dimitriou, Evangelia, Paschali, Evangelia, Kanariou, Maria, Michelakakis, Helen
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Elsevier 2019
Materias:
Research Paper
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6554541/
https://www.ncbi.nlm.nih.gov/pubmed/31194046
http://dx.doi.org/10.1016/j.ymgmr.2019.100477

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6554541/
https://www.ncbi.nlm.nih.gov/pubmed/31194046
http://dx.doi.org/10.1016/j.ymgmr.2019.100477

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