K Misu

Mechanisms of autophagy–lysosome dysfunction in neurodegenerative diseases

Cardiac Amyloidosis Due to Transthyretin Protein

An axonal form of Charcot-Marie-Tooth disease showing distinctive features in association with mutations in the peripheral myelin protein zero gene (Thr124Met or Asp75Val)

Late-onset familial amyloid polyneuropathy type I (transthyretin Met30-associated familial amyloid polyneuropathy) unrelated to endemic focus in Japan