The Human Lipodystrophy Gene BSCL2/Seipin May Be Essential for Normal Adipocyte Differentiation

OBJECTIVE—Berardinelli-Seip congenital lipodystrophy type 2 (BSCL2) is a recessive disorder featuring near complete absence of adipose tissue. Remarkably, although the causative gene, BSCL2, has been known for several years, its molecular function and its role in adipose tissue development have not...

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Detalles Bibliográficos
Autores principales: Payne, Victoria A., Grimsey, Neil, Tuthill, Antoinette, Virtue, Sam, Gray, Sarah L., Nora, Edoardo Dalla, Semple, Robert K., O'Rahilly, Stephen, Rochford, Justin J.
Formato: Texto
Lenguaje:English
Publicado: American Diabetes Association 2008
Materias:
Metabolism
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2494687/
https://www.ncbi.nlm.nih.gov/pubmed/18458148
http://dx.doi.org/10.2337/db08-0184

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2494687/
https://www.ncbi.nlm.nih.gov/pubmed/18458148
http://dx.doi.org/10.2337/db08-0184

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