Bscl2 Deficiency Does Not Directly Impair the Innate Immune Response in a Murine Model of Generalized Lipodystrophy

Congenital Generalized Lipodystrophy type 2 (CGL2) is the most severe form of lipodystrophy and is caused by mutations in the BSCL2 gene. Affected patients exhibit a near complete lack of adipose tissue and suffer severe metabolic disease. A recent study identified infection as a major cause of deat...

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Detalles Bibliográficos
Autores principales: Roumane, Ahlima, Mcilroy, George D., Balci, Arda, Han, Weiping, Delibegović, Mirela, Baldassarre, Massimiliano, Newsholme, Philip, Rochford, Justin J.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2021
Materias:
Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7865406/
https://www.ncbi.nlm.nih.gov/pubmed/33498782
http://dx.doi.org/10.3390/jcm10030441

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7865406/
https://www.ncbi.nlm.nih.gov/pubmed/33498782
http://dx.doi.org/10.3390/jcm10030441

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