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

Author:

Yamada Yumi1,Fukushima Takao1,Kodama Satoshi2,Shimizu Hiroshi3,Kakita Akiyoshi3,Makino Kunihiko1,Sekijima Yoshiki2

Affiliation:

1. Department of Neurology, Niigata Prefectural Shibata Hospital, Shibata, Japan

2. Department of Medicine (Neurology and Rheumatology), Shinshu University School of Medicine, Matsumoto, Japan

3. Department of Pathology, Brain Research Institute, Niigata University, Niigata, Japan

Funder

Grant-in-aid for Scientific Research

Amyloidosis Research Committee, the Ministry of Health, Labour and Welfare, Japan

Publisher

Informa UK Limited

Subject

Internal Medicine

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