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Clinical and histopathological features of familial amyloidotic polyneuropathy with transthyretin Val30Ala in a Chinese family

✍ Scribed by Jing-Yao Liu; Ying-Jie Guo; Chun-Kui Zhou; Yu-Qin Ye; Jun-Qiang Feng; Fei Yin; Xin-Mei Jiang


Book ID
119304006
Publisher
Elsevier Science
Year
2011
Tongue
English
Weight
203 KB
Volume
304
Category
Article
ISSN
0022-510X

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Amyloidosis is characterised by the extracellular deposition of certain different proteins in a distinctively abnormal fibrillar conformation. All types of amyloid fibril share remarkably similar structural and biophysical properties despite substantial chemical heterogeneity among their respective