Common origin of the Val30Met mutation responsible for the amyloidogenic transthyretin type of familial amyloidotic polyneuropathy

Benzer Materyaller

• Vasculopathy in transthyretin Val30Met familial amyloid polyneuropathy
  Yazar:: Koike, Haruki, ve diğerleri
  Baskı/Yayın Bilgisi: (2015)
• Deposition of Transthyretin in Early Stages of Familial Amyloidotic Polyneuropathy : Evidence for Toxicity of Nonfibrillar Aggregates
  Yazar:: Mendes Sousa, Mónica, ve diğerleri
  Baskı/Yayın Bilgisi: (2001)
• Amyloid fibril protein in familial amyloidotic polyneuropathy, Portuguese type. Definition of molecular abnormality in transthyretin (prealbumin).
  Yazar:: Saraiva, M J, ve diğerleri
  Baskı/Yayın Bilgisi: (1984)
• Biochemical marker in familial amyloidotic polyneuropathy, Portuguese type. Family studies on the transthyretin (prealbumin)-methionine-30 variant.
  Yazar:: Saraiva, M J, ve diğerleri
  Baskı/Yayın Bilgisi: (1985)
• Familial amyloidotic polyneuropathy without familial occurrence: carrier detection by the radioimmunoassay of variant transthyretin.
  Yazar:: Tanaka, M, ve diğerleri
  Baskı/Yayın Bilgisi: (1988)