Proteomic Evidence of Biological Aging in a Child with a Compound Heterozygous ZMPSTE24 Mutation

Documenti analoghi

• Homozygous and compound heterozygous mutations in ZMPSTE24 cause the laminopathy restrictive dermopathy
  di: Moulson, Casey L., et al.
  Pubblicazione: (2005)
• Early Onset Mandibuloacral Dysplasia due to Compound Heterozygous Mutations in ZMPSTE24
  di: Ahmad, Zahid, et al.
  Pubblicazione: (2010)
• Severe mandibuloacral dysplasia caused by novel compound heterozygous ZMPSTE24 mutations in two Japanese siblings
  di: Miyoshi, Y, et al.
  Pubblicazione: (2008)
• Compound heterozygous ZMPSTE24 mutations reduce prelamin A processing and result in a severe progeroid phenotype
  di: Shackleton, S, et al.
  Pubblicazione: (2005)
• A Heterozygous ZMPSTE24 Mutation Associated with Severe Metabolic Syndrome, Ectopic Fat Accumulation, and Dilated Cardiomyopathy
  di: Galant, Damien, et al.
  Pubblicazione: (2016)