Genetic study of transthyretin amyloid neuropathies: carrier risks among French and Portuguese families

Documenti analoghi

• Transthyretin gene mutations in British and French patients with amyloid neuropathy.
  di: Bhatia, K, et al.
  Pubblicazione: (1993)
• TTR familial amyloid polyneuropathy: does a mitochondrial polymorphism entirely explain the parent-of-origin difference in penetrance?
  di: Bonaïti, Bernard, et al.
  Pubblicazione: (2010)
• Strategies to improve the quality of life in patients with hereditary transthyretin amyloidosis (hATTR) and autonomic neuropathy
  di: Gendre, Thierry, et al.
  Pubblicazione: (2019)
• Heterogeneity of penetrance in familial amyloid polyneuropathy, ATTR Val30Met, in the Swedish population
  di: Hellman, Urban, et al.
  Pubblicazione: (2008)
• An exclusion map covering the whole genome: a new challenge for genetic epidemiologists?
  di: Clerget-Darpoux, F, et al.
  Pubblicazione: (1993)