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    Clinical features and haplotype analysis of newly identified Japanese patients with gelsolin-related familial amyloidosis of Finnish type

    Familial amyloidosis of the Finnish type (FAF) is an autosomal dominant form of systematic amyloidosis characterized by lattice corneal dystrophy, cranial neuropathy, and cutis laxa. Although FAF has been frequen...

    Makiko Taira, Hiroyuki Ishiura, Jun Mitsui, Yuji Takahashi… in neurogenetics (2012)