Familial amyloid polyneuropathy with chronic paroxysmal dry cough in Mainland China: A Chinese family with a proven heterozygous missense mutation c.349G>T in the transthyretin gene-Reference-Cited by-同舟云学术

Familial amyloid polyneuropathy with chronic paroxysmal dry cough in Mainland China: A Chinese family with a proven heterozygous missense mutation c.349G>T in the transthyretin gene

Published:2019-02 Issue: Volume:60 Page:164-166
ISSN:0967-5868
Container-title:Journal of Clinical Neuroscience
language:en
Short-container-title:Journal of Clinical Neuroscience

Author:

Yuan Zhenhua,Guo Lina,Liu Xixi,Xiao Xuewen,Jiao Bin,Wang Junling,Yan Xinxiang,Tang Beisha,Shen Lu

Funder

National Natural Science Foundation of China

Publisher

Elsevier BV

Subject

Physiology (medical),Neurology (clinical),Neurology,General Medicine,Surgery

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1. Clinical and molecular insights into A97S variants in hereditary transthyretin amyloid polyneuropathy in South China;Amyloid;2024-07-31

2. Negative methylene diphosphonate scintigraphy in biopsy-confirmed hereditary transthyretin Ala117Ser cardiac amyloidosis: a case report;Cardiology Plus;2023-07

3. Clinical and biochemical characterization of hereditary transthyretin amyloidosis caused by E61K mutation;Frontiers in Molecular Neuroscience;2022-10-12

4. Clinical phenotypes and genetic features of hereditary transthyretin amyloidosis patients in China;Orphanet Journal of Rare Diseases;2022-09-02

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