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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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| Главные авторы: | , , , , , , , , , , , , |
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| Формат: | Artigo |
| Язык: | Inglês |
| Опубликовано: |
BioMed Central
2013
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| Предметы: | |
| Online-ссылка: | 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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