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...

Täydet tiedot

Tallennettuna:
Bibliografiset tiedot
Päätekijät: 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
Aineistotyyppi: Artigo
Kieli:Inglês
Julkaistu: BioMed Central 2013
Aiheet:
Research
Linkit: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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