Unique molecular signature in mucolipidosis type IV microglia

BACKGROUND: Lysosomal storage diseases (LSD) are a large family of inherited disorders characterized by abnormal endolysosomal accumulation of cellular material due to catabolic enzyme and transporter deficiencies. Depending on the affected metabolic pathway, LSD manifest with somatic or central ner...

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Detalles Bibliográficos
Autores principales: Cougnoux, Antony, Drummond, Rebecca A., Fellmeth, Mason, Navid, Fatemeh, Collar, Amanda L., Iben, James, Kulkarni, Ashok B., Pickel, James, Schiffmann, Raphael, Wassif, Christopher A., Cawley, Niamh X., Lionakis, Michail S., Porter, Forbes D.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2019
Materias:
Research
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6935239/
https://www.ncbi.nlm.nih.gov/pubmed/31883529
http://dx.doi.org/10.1186/s12974-019-1672-4

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6935239/
https://www.ncbi.nlm.nih.gov/pubmed/31883529
http://dx.doi.org/10.1186/s12974-019-1672-4

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