A mutation in the c-Fos gene associated with congenital generalized lipodystrophy

BACKGROUND: Congenital generalized lipodystrophy (CGL) or Berardinelli–Seip congenital lipodystrophy (BSCL) is a rare genetic syndrome characterized by the absence of adipose tissue. As CGL is thought to be related to malfunctions in adipocyte development, genes involved in the mechanisms of adipocy...

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Detalhes bibliográficos
Main Authors: Knebel, Birgit, Kotzka, Jorg, Lehr, Stefan, Hartwig, Sonja, Avci, Haluk, Jacob, Sylvia, Nitzgen, Ulrike, Schiller, Martina, März, Winfried, Hoffmann, Michael M, Seemanova, Eva, Haas, Jutta, Muller-Wieland, Dirk
Formato: Artigo
Idioma:Inglês
Publicado em: BioMed Central 2013
Assuntos:
Research
Acesso em linha:https://ncbi.nlm.nih.gov/pmc/articles/PMC3750569/
https://ncbi.nlm.nih.gov/pubmed/23919306
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1186/1750-1172-8-119
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