Literature DB >> 10923048

Transthyretin Ala97Ser is associated with familial amyloidotic polyneuropathy in a Chinese-Taiwanese family.

H J Lachmann1, D R Booth, A Bybee, P N Hawkins.   

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Year:  2000        PMID： 10923048     DOI： 10.1002/1098-1004(200008)16:2<180::AID-HUMU19>3.0.CO;2-A

Source DB:  PubMed          Journal:  Hum Mutat        ISSN： 1059-7794            Impact factor:   4.878


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  3 in total

1.  Multimodal retinal imaging in a Chinese kindred with familial amyloid polyneuropathy secondary to transthyretin Ile107Met mutation.

Authors:  W Lv; J Chen; W Chen; P Hou; C P Pang; H Chen
Journal:  Eye (Lond)       Date:  2014-01-31       Impact factor: 3.775

2.  Ala97Ser transthyretin amyloidosis-associated polyneuropathy, clinical and neurophysiological profiles in a Thai cohort.

Authors:  Nath Pasutharnchat; Chamaiporn Taychargumpoo; Yongkasem Vorasettakarnkij; Jakkrit Amornvit
Journal:  BMC Neurol       Date:  2021-05-22       Impact factor: 2.474

3.  Mutation p.G83R in the transthyretin gene is associated with hereditary vitreous amyloidosis in Han Chinese families.

Authors:  A-Mei Zhang; Hui Wang; Peng Sun; Qiu-Xiang Hu; Yuqing He; Yong-Gang Yao
Journal:  Mol Vis       Date:  2013-07-25       Impact factor: 2.367
  3 in total

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