The Val142Ile transthyretin cardiac amyloidosis: more than an Afro-American pathogenic variant

Ítems similars

• Syncope as a Phenotypic Expression of Hereditary Transthyretin Amyloidosis Val142Ile (Val122Ile)
  per: Nágela S. V. Nunes, et al.
• A case of cardiac amyloidosis in an elderly Japanese patient with amyloidogenic transthyretin Val122Ile variant
  per: Ono, Ryohei, et al.
  Publicat: (2020)
• Síncope como Expressão Fenotípica da Amiloidose Hereditária por Transtirretina Val142Ile (Val122Ile)
  per: Nunes, Nágela S. V., et al.
  Publicat: (2020)
• Cardiac Findings and Events Observed in an Open-Label Clinical Trial of Tafamidis in Patients with non-Val30Met and non-Val122Ile Hereditary Transthyretin Amyloidosis
  per: Damy, Thibaud, et al.
  Publicat: (2015)
• Transthyretin Val30Met Mutation in an African American with Cardiac Amyloidosis
  per: Schulze, P. Christian, et al.
  Publicat: (2010)