[Hereditary amyloidosis]

Nouv Presse Med. 1972 Oct 28;1(38):2525-8.
[Article in French]
No abstract available

MeSH terms

  • Amyloidosis / genetics*
  • Chromosome Aberrations
  • Chromosome Disorders
  • Deafness / genetics
  • Familial Mediterranean Fever / genetics*
  • Fibrinogen
  • Heart Failure / genetics
  • Humans
  • Joint Diseases / genetics
  • Neurologic Manifestations
  • Pain / genetics
  • Peripheral Nervous System Diseases / genetics
  • Peritonitis / genetics
  • Polyneuropathies / genetics
  • Portugal
  • Prognosis
  • Racial Groups
  • Skin Diseases / genetics
  • Thyroid Neoplasms / genetics

Substances

  • Fibrinogen