Hereditary transthyretin amyloidosis associated with a transthyretin variant Thr59Arg

Autor:	Masayoshi Tasaki, Tetsuya Watanabe, Konen Obayashi, Tomotaka Ando, Yukio Ando, Takafumi Akagami, Shinichi Hirotani, Yohei Misumi, Taro Yamashita, Satoru Shinriki, Mitsuharu Ueda
Rok vydání:	2017
Předmět:	0301 basic medicine Male Pathology medicine.medical_specialty Amyloid 030105 genetics & heredity 03 medical and health sciences 0302 clinical medicine Internal Medicine Medicine Humans Prealbumin Gastrointestinal tract Amyloid Neuropathies Familial biology business.industry Amyloidosis nutritional and metabolic diseases Middle Aged medicine.disease Transthyretin Mutation biology.protein business Cardiomyopathies 030217 neurology & neurosurgery
Zdroj:	Amyloid : the international journal of experimental and clinical investigation : the official journal of the International Society of Amyloidosis. 24(sup1)
ISSN:	1744-2818
Popis:	Hereditary transthyretin (TTR) amyloidosis is characterized by ATTR amyloid deposits in various tissue sites and organs, such as peripheral nerves, heart, gastrointestinal tract, kidneys, eyes, and...
Databáze:	OpenAIRE
Externí odkaz:	https://explore.openaire.eu/search/publication?articleId=doi_dedup___::280e2f717a4b4627304b31392b24b437 https://pubmed.ncbi.nlm.nih.gov/28434332 Zobrazit plný text záznamu