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Amyloid
The Journal of Protein Folding Disorders
Volume 26, 2019 - Issue 4
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Letters to the Editor

A case of cerebral amyloid angiopathy-type hereditary ATTR amyloidosis with Y69H (p.Y89H) variant displaying transient focal neurological episodes as the main symptom

Yumi YamadaDepartment of Neurology, Niigata Prefectural Shibata Hospital, Shibata, JapanView further author information
,
Takao FukushimaDepartment of Neurology, Niigata Prefectural Shibata Hospital, Shibata, JapanView further author information
,
Satoshi KodamaDepartment of Medicine (Neurology and Rheumatology), Shinshu University School of Medicine, Matsumoto, JapanView further author information
,
Hiroshi ShimizuDepartment of Pathology, Brain Research Institute, Niigata University, Niigata, JapanView further author information
,
Akiyoshi KakitaDepartment of Pathology, Brain Research Institute, Niigata University, Niigata, JapanView further author information
,
Kunihiko MakinoDepartment of Neurology, Niigata Prefectural Shibata Hospital, Shibata, JapanView further author information
&
Yoshiki SekijimaDepartment of Medicine (Neurology and Rheumatology), Shinshu University School of Medicine, Matsumoto, JapanCorrespondence[email protected]
View further author information
 show all
Pages 251-252 | Received 19 Mar 2019, Accepted 13 Jun 2019, Published online: 01 Jul 2019
 
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"A case of cerebral amyloid angiopathy-type hereditary ATTR amyloidosis with Y69H (p.Y89H) variant displaying transient focal neurological episodes as the main symptom." Amyloid, 26(4), pp. 251–252

Disclosure statement

No potential conflict of interest was reported by the authors.

Additional information

Funding

This study was supported by a Grant-in-aid for Scientific Research (19K07959 to Y.S.) and a grant from the Amyloidosis Research Committee, the Ministry of Health, Labour and Welfare, Japan.

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