Association Between Nuclear Lamin A/C R482Q Mutation and Partial Lipodystrophy with Hyperinsulinemia, Dyslipidemia, Hypertension, and Diabetes

Lignende værker

• Obstructive sleep apnea in 2 women with familial partial lipodystrophy due to a heterozygous LMNA R482Q mutation
  af: Hegele, Robert A., et al.
  Udgivet: (2007)
• Structure of the lamin A/C R482W mutant responsible for dominant familial partial lipodystrophy (FPLD)
  af: Magracheva, Eugenia, et al.
  Udgivet: (2009)
• Heterozygous CAV1 frameshift mutations (MIM 601047) in patients with atypical partial lipodystrophy and hypertriglyceridemia
  af: Cao, Henian, et al.
  Udgivet: (2008)
• Sequencing of the Reannotated LMNB2 Gene Reveals Novel Mutations in Patients with Acquired Partial Lipodystrophy
  af: Hegele, Robert A., et al.
  Udgivet: (2006)
• Unbuckling lipodystrophy from insulin resistance and hypertension
  af: Hegele, Robert A., et al.
  Udgivet: (2004)