Amyloid

The Journal of Protein Folding Disorders

Volume 23, 2016 - Issue 3

137

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Letter to the Editor

Hereditary amyloidosis with cardiomyopathy caused by the novel variant transthyretin A36D

Taro YamashitaDepartment of Neurology, Graduate School of Medical Sciences, Kumamoto University, Kumamoto, Japan, ;Diagnostic Unit for Amyloidosis, Kumamoto University Hospital, Kumamoto, Japan, Correspondence[email protected]

Mitsuharu UedaDepartment of Neurology, Graduate School of Medical Sciences, Kumamoto University, Kumamoto, Japan,

Nobuyuki SagaDepartment of Nephrology,

Kiyonori NantoDepartment of Cardiology, Kansai Rosai Hospital, Amagasaki, Japan,

Masayoshi TasakiDepartment of Neurology, Graduate School of Medical Sciences, Kumamoto University, Kumamoto, Japan,

Teruaki MasudaDepartment of Neurology, Graduate School of Medical Sciences, Kumamoto University, Kumamoto, Japan,

Yohei MisumiDepartment of Neurology, Graduate School of Medical Sciences, Kumamoto University, Kumamoto, Japan,

Seitaro OdaDepartment of Diagnostic Radiology,

Akiko FujimotoDepartment of Neurology, Graduate School of Medical Sciences, Kumamoto University, Kumamoto, Japan,

Tomoko AmanoDepartment of Neurology, Graduate School of Medical Sciences, Kumamoto University, Kumamoto, Japan,

Kotaro TakamatsuDepartment of Neurology, Graduate School of Medical Sciences, Kumamoto University, Kumamoto, Japan,

Satoshi YamashitaDepartment of Neurology, Graduate School of Medical Sciences, Kumamoto University, Kumamoto, Japan,

Konen ObayashiDepartment of Molecular Laboratory Medicine, and

Hirotaka MatsuiDepartment of Morphological and Physiological Sciences, Graduate School of Medical Sciences, Kumamoto University, Kumamoto, Japan

Yukio AndoDepartment of Neurology, Graduate School of Medical Sciences, Kumamoto University, Kumamoto, Japan,

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"Hereditary amyloidosis with cardiomyopathy caused by the novel variant transthyretin A36D." Amyloid, 23(3), pp. 207–208

Declaration of interest

The authors report no conflicts of interest.

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Hereditary amyloidosis with cardiomyopathy caused by the novel variant transthyretin A36D

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Hereditary amyloidosis with cardiomyopathy caused by the novel variant transthyretin A36D

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