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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Detalhes bibliográficos
Publicado no:J Neuroinflammation
Main Authors: 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: Artigo
Idioma:Inglês
Publicado em: BioMed Central 2019
Assuntos:
Research
Acesso em linha:https://ncbi.nlm.nih.gov/pmc/articles/PMC6935239/
https://ncbi.nlm.nih.gov/pubmed/31883529
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1186/s12974-019-1672-4
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