Clinical features of familial amyloid polyneuropathy carrying transthyretin mutations in four Chinese kindreds-Reference-Cited by-同舟云学术

Clinical features of familial amyloid polyneuropathy carrying transthyretin mutations in four Chinese kindreds

Published:2017-03 Issue:1 Volume:22 Page:19-26
ISSN:1085-9489
Container-title:Journal of the Peripheral Nervous System
language:en
Short-container-title:J Peripher Nerv Syst

Author:

Liu Gonglu¹,Ni Wang¹,Wang Hongxia²,Li Hongfu¹,Zhang Yue³,Wang Ning⁴,Wu Zhiying¹

Affiliation:

1. Department of Neurology and Research Center of Neurology, Collaborative Innovation Center for Brain Science; Zhejiang University School of Medicine Second Affiliated Hospital; Hangzhou China

2. Department of Neurology; First Affiliated Hospital of Soochow University; Suzhou China

3. Department of Neurology, Institute of Neurology; Huashan Hospital Fudan University; Shanghai China

4. Department of Neurology, Institute of Neurology; First Affiliated Hospital of Fujian Medical University; Fuzhou China

Publisher

Wiley

Subject

Clinical Neurology,General Neuroscience

Link

http://onlinelibrary.wiley.com/wol1/doi/10.1111/jns.12196/fullpdf

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4. Transthyretin Arg-83 mutation in vitreous amyloidosis;Chen;Int J Ophthalmol,2011

5. Exome sequencing and gene prioritization correct misdiagnosis in a Chinese kindred with familial amyloid polyneuropathy;Chen;Sci Rep,2016

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