The strange case of the ‘lumper’ lamin A/C gene and human premature ageing

This publication has 23 references indexed in Scilit:

• Lamin A Truncation in Hutchinson-Gilford Progeria
  Science, 2003
• A progeroid syndrome in mice is caused by defects in A-type lamins
  Nature, 2003
• Recurrent de novo point mutations in lamin A cause Hutchinson–Gilford progeria syndrome
  Nature, 2003
• LMNA is mutated in Hutchinson-Gilford progeria (MIM 176670) but not in Wiedemann-Rautenstrauch progeroid syndrome (MIM 264090)
  Journal of Human Genetics, 2003
• Discovering genotypes underlying human phenotypes: past successes for mendelian disease, future approaches for complex disease
  Nature Genetics, 2003
• An allelic series of mutations in Smad2 and Smad4 identified in a genotype-based screen of N -ethyl- N - nitrosourea-mutagenized mouse embryonic stem cells
  Proceedings of the National Academy of Sciences, 2002
• Molecular diagnosis of cystic fibrosis
  Expert Review of Molecular Diagnostics, 2002
• Mutations in the p53 homolog p63: allele-specific developmental syndromes in humans
  Trends in Molecular Medicine, 2002
• Lumping and splitting: molecular biology in the genetics clinic
  Clinical Genetics, 1998
• Bone dysplasias in man: molecular insights
  Current Opinion in Genetics & Development, 1996