Transthyretin Tyr69-to-Ile mutation (doublenucleotide substitution in codon 69) in a Japanese familial amyloidosis patient with cardiomyopathy and carpal tunnel syndrome

Yo-Ichi Takei Third Department of Medicine, Shinshu University School of Medicine, 3–1-1 Asahi, Matsumoto, 390–8621, JapanCorrespondence[email protected]

Takeshi Hattori Third Department of Medicine, Shinshu University School of Medicine, 3–1-1 Asahi, Matsumoto, 390–8621, Japan

Masahide Yazaki Third Department of Medicine, Shinshu University School of Medicine, 3–1-1 Asahi, Matsumoto, 390–8621, Japan

Takahiko Tokuda Third Department of Medicine, Shinshu University School of Medicine, 3–1-1 Asahi, Matsumoto, 390–8621, Japan

Nobuyuki Urasawa Third Department of Medicine, Shinshu University School of Medicine, 3–1-1 Asahi, Matsumoto, 390–8621, Japan

Shinichiro Kanai Third Department of Medicine, Shinshu University School of Medicine, 3–1-1 Asahi, Matsumoto, 390–8621, Japan

Shu-Ichi Ikeda Third Department of Medicine, Shinshu University School of Medicine, 3–1-1 Asahi, Matsumoto, 390–8621, Japan

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Transthyretin Tyr69-to-Ile mutation (doublenucleotide substitution in codon 69) in a Japanese familial amyloidosis patient with cardiomyopathy and carpal tunnel syndrome

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Transthyretin Tyr69-to-Ile mutation (doublenucleotide substitution in codon 69) in a Japanese familial amyloidosis patient with cardiomyopathy and carpal tunnel syndrome

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